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Werner syndrome helicase - Wikipedi

Werner syndrome - Simple English Wikipedia, the free

  1. al and pelvic organs. It is a type of abnormality of the Müllerian ducts
  2. Wernicke-Korsakoff syndrome. Wernicke-Korsakoff syndrome ( WKS) is the combined presence of Wernicke encephalopathy (WE) and Korsakoff syndrome. Due to the close relationship between these two disorders, people with either are usually diagnosed with WKS as a single syndrome. It mainly causes vision changes, ataxia and impaired memory
  3. Werner syndrome is characterized by the dramatic, rapid appearance of features associated with normal aging. Individuals with this disorder typically grow and develop normally until they reach puberty. Affected teenagers usually do not have a growth spurt, resulting in short stature

Werner syndrome, also called progeria, is a hereditary condition associated with premature aging and an increased risk of cancer and other diseases. Signs of Werner syndrome usually develop in the childhood or teenage years Bloom syndrome (often abbreviated as BS in literature) is a rare autosomal recessive genetic disorder characterized by short stature, predisposition to the development of cancer, and genomic instability. BS is caused by mutations in the BLM gene which is a member of the RecQ DNA helicase family. Mutations in other members of this family, namely WRN and RECQL4, are associated with the clinical.

Werner Syndrome: What Is It?-Werner Syndrome is a mutation of the WRN gene.-The WRN gene is a helicase enzyme which separates and unwindsdouble stranded DNA, which is necessary for DNA to be copied for celldivision.-It is also responsible for making the blue print of a gene for proteinproduction.-Lastly, it's also believed to play a role in repairing DNA Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Werner syndrome. PubMed provides review articles from the past five years (limit to free review articles

Wagner syndrome is an autosomal dominant vitreoretinopathy that results in a variety of ocular findings. The characteristic feature of the syndrome is an optically empty vitreous. Myopia, presenile cataract, and night blindness are also commonly associated findings Werner syndrome Information on Healthline - ウェイバックマシン(2011年9月15日アーカイブ分) この項目は、 医学 に関連した 書きかけの項目 です。 この項目を加筆・訂正 などしてくださる 協力者を求めています ( プロジェクト:医学 / Portal:医学と医療 ) Wiedemann-Rautenstrauch (WR) syndrome ([ˈviːdəman ˈʁa͜ʊtən.ʃtʁa͜ʊx]), also known as neonatal progeroid syndrome, is a rare autosomal recessive progeroid syndrome. There have been over 30 cases of WR. WR is associated with abnormalities in bone maturation, and lipids and hormone metabolism Otto Werner originally defined Werner syndrome (WS) in 1904 on the basis of sclerodermalike, thin, tight skin and bilateral cataracts. WS is also known as progeria adultorum, progeria of the adult,..

베르너 증후군(Werner syndrome)은 일반 사람보다 몇 배의 속도로 나이가 드는 '조기노화증'(早期老化症)의 하나이다.한국에서는 조로증(早老症)으로 많이 알려져 있다.. 1904년 독일 안과 의사인 오토 베르너(Otto Werner)가 발견하여 그의 이름을 따 '베르너 증후군'이라고 칭하였다 Herlyn-Werner-Wunderlich (HWW) syndrome is characterized by a triad of type III Müllerian duct anomaly (uterus didelphys), obstructed hemivagina and mesonephric duct anomalies. Most often the latter manifests as renal agenesis 3 but duplicated kidneys, dysplastic kidneys, rectovesical bands or crossed fused ectopia may also be seen

Werner syndrome - wikido

  1. Werner syndrome. Definition from Wiktionary, the free dictionary. Jump to navigation Jump to search. English . English Wikipedia has an article on: Werner syndrome. Wikipedia . Etymology . Named after the German scientist Otto Werner. Noun . Werner syndrome (uncountable
  2. Werner syndrome is a genetic condition. This means that the risk of Werner syndrome can be passed from generation to generation in a family. Mutations (alterations) in the WRN gene are known to cause Werner syndrome. Research is ongoing to learn more about Werner syndrome
  3. Rothmund-T syndrome is a rare genetic disorder that manifests in early infancy. The range and severity of symptoms may vary from case to case. RTS is typically characterized by skin rash, sparse hair, malformed bones, abnormal clouding of the lenses of the eyes (juvenile cataracts), small stature, and other physical abnormalities
  4. Chelsea Werner is a fashion model, Special Olympian, and a groundbreaking young woman. There is no denying that this beauty has defied physical and professional odds. Her work ethics are intimidating. This model has become a symbol for people who have been suffering from Down's Syndrome
  5. Síndrome de Werner, também chamada de velhice precoce, é uma doença genética que faz com que o portador envelheça 5 a 10 vezes mais rapidamente que o normal.Foi descoberta por Otto Werner.Esta doença resulta na acumulação de lesões no DNA, pois o produto do gene defeituoso é a DNA helicase - uma proteína envolvida na replicação e reparação do DNA
  6. Although the delivery is successful, the baby is premature, born after only ten weeks of pregnancy, and is diagnosed with an exaggerated form of Werner syndrome (an aging disease) as stated by Dr. Benfante (Allan Rich) and Dr. Lin (Keone Young)

Werner syndrome. A rare autosomal recessive progeroid syndrome (OMIM:277700) characterised by premature onset of multiple age-related disorders, including atherosclerosis, cancer, type-2 diabetes, ocular cataracts, osteoporosis, and death by age 47, often due to myocardial infarction. Defects of WRN, which encodes a DNA helicase responsible for. Werner syndrome (WS) is an inherited disorder that produces somatic stunting, premature ageing and early onset of degenerative and neoplastic diseases. Cultured fibroblasts derived from subjects with WS are found to undergo premature replicative senescence and thus provide a cellular model system to study the disorder The Relationship between Werner Syndrome and Sinonasal Malignant Melanoma: Two Sibling Cases of Werner Syndrome with Malignant Melanoma To do this, they created a cellular model of Werner syndrome by using a cutting-edge gene-editing technology to delete WRN gene in human stem cells Werner syndrome (WS) is an uncommon autosomal recessive disorder characterized by premature aging. The clinical manifestations of WS, including atherosclerosis and osteoporosis, appear early in adulthood, and death in the fourth to sixth decade commonly ensues from myocardial infarction or cancer

LMNA: The Root of Progeria - Home

OHVIRA - Wikipedi

Wernicke-Korsakoff syndrome - Wikipedi

werner syndrome. Ze!Converter - Download Video From Dailymotion to mp4, mp3, aac, m4a, f4v, or 3gp for free! werner syndrome - this is an unpleasant disease. The photos of werner syndrome below are not recommended for people with a weak psyche! We wish you a cure and never get sick of this disease This Inspiring Girl With Down Syndrome Is An Olympic Champion (Chelsea Werner) Posted by David Wolfe on Wednesday, November 15, 2017. Girl With Down Syndrome Defies All Stereotypes. When Chelsea was born with Down Syndrome, no one thought she'd accomplish much - 20 years later, she defies all stereotypes There is, of course, the exceptions and two-time defending World Champion Chelsea Werner might be as good as it gets. Chelsea was born with Down Syndrome, unable to walk until she was almost two. Werner's syndrome synonyms, Werner's syndrome pronunciation, Werner's syndrome translation, English dictionary definition of Werner's syndrome. or Wer·ner's syndrome n. An autosomal recessive disorder characterized by short stature and the appearance of premature aging after puberty, with early..

Werner syndrome: MedlinePlus Genetic

Individuals with Werner syndrome develop normally until the end of the first decade. The first sign is the lack of a growth spurt during the early teen years. Early findings (usually observed in the 20s) include loss and graying of hair, hoarseness, and scleroderma-like skin changes, followed by bilateral ocular cataracts, type 2 diabetes. 6659. WRN Викиҗыентыкта. WRN ( ингл. Werner syndrome RecQ like helicase [d]) — кешенең 8-нче хромосомасы [d] аксымы, шул ук исемдәге ген тарафыннан кодлана торган югары молекуляр органик матдә

Werner Syndrome Cancer

Bloom syndrome - Wikipedi

  1. Carl Wilhelm Otto Werner (born February 1, 1879 in Flensburg, † June 5, 1936 in Eddelak, Schleswig-Holstein) was a German medic. He became famous for his studies on premature aging. The Werner Syndrome was named after him
  2. The Eaton McKusick syndrome is a hereditary malformation syndrome with a combination of limb malformations, it is named after the American geneticists GO Eaton and Victor A. McKusick.. It was first described in 1919 by the Austrian gynecologist Paul Werner, hence the name mesomelic dysplasia or Werner syndrome, but not to be confused with Werner syndrome (adult progeria)
  3. Werner syndrome is an autosomal recessive disorder; carriers of (only) one mutation are generally considered to be unaffected, as only carriers of two mutations exhibit the clinical signs of progeria . The most common WRN mutation in Caucasians, and the second most common in Japanese, is rs17847577 (T). Another mutation is also common among.
  4. Werner: Clean scrolling into 8 directions. The sound is also successful. But right from the start the game has a very high difficulty grade. 8 points. Miscellaneous [edit | edit source] Originally, Alien Syndrome was issued on the Amiga and was later converted to this version on the C64. Cove
  5. Lynch syndrome is a genetic disorder that causes an increased risk of developing certain types of cancer such as colon and rectal cancer, as well as cancers of the stomach, small intestine, liver, gallbladder ducts, upper urinary tract, brain, skin, and prostate. Women with Lynch syndrome also have a high risk of developing uterine cancer (also called endometrial cancer) and ovarian cancer

WRN ( Vernerov sindrom) je ljudski gen koji korira Vernerov protein. On je helikaza. Helikaze su enzimi koji generalno odvijaju i razdvajaju lance dvolančane DNK. Te aktivnosti su neophodne pre kopiranja DNK u pripremi za ćelijsku deobu ( DNK ). Helikaze su takođe kritične u procesu transkripcije Congenital adrenal hyperplasia (CAH) Congenital Central Hypoventilation Syndrome. Congenital Diaphragmatic Hernia (CDH) Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins. Costello syndrome. Craniopagus parasiticus. Cri du chat syndrome Patients with Werner syndrome will display rapid premature aging beginning in young adulthood, usually in their early twenties. en.wikipedia.org While normal atherosclerosis generally involves the major arteries, smaller arterioles are more likely to be affected in Werner syndrome patients

Werner's syndrome: [ ver´nerz ] premature aging in the adult, transmitted as an autosomal recessive trait, and characterized principally by sclerodermalike skin changes, involving especially the extremities, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, white hair and/or. Synonyms for Werner's syndrome in Free Thesaurus. Antonyms for Werner's syndrome. 7 synonyms for syndrome: condition, complaint, illness, symptoms, disorder, ailment, affliction. What are synonyms for Werner's syndrome

Werner syndrome - SlideShar

  1. ate any im
  2. Media in category Werner syndrome ATP-dependent helicase, WRN. The following 7 files are in this category, out of 7 total. PBB GE WRN 205667 at fs.png 732 × 530; 11 KB. PBB GE WRN 205667 at tn.png 255 × 135; 853 bytes. PDB 2dgz EBI.jpg 800 × 600; 36 KB
  3. Multiple Endocrine Neoplasia (MEN-1) was originally known as Wermer syndrome. The most common tumors seen in MEN-1 involve the parathyroid gland, islet cells of the pancreas, and pituitary gland. Creatinine level greater than 2.5 mg indicates stage 3 or more advance CKD eGFR 34.4 ml/L.Diagnosed or suspected endocrine diseases like Cushing.
  4. Werner syndrome A rare autosomal recessive progeroid syndrome (OMIM:277700) characterised by premature onset of multiple age-related disorders, including atherosclerosis, cancer, type-2 diabetes, ocular cataracts, osteoporosis, and death by age 47, often due to myocardial infarction
  5. Werner syndrome, a genetic disorder also called adult progeria, leads to graying hair, cataracts, osteoporosis and other signs of aging in people in their 20s. DNA disorganization promotes aging: changes result in cell chaos that causes gray hair, brittle bone
  6. al Minds, Dorado Falls. 1 Background 2 Dorado Falls 3 Modus Operandi 4 Profile 5 Known Victims 6 Notes 7 Appearances Dolan was born sometime around 1974. On March 23, 1998, he married a woman named Jenna Moxon, with whom he had a.

Talk:Werner syndrome - Wikipedi

  1. Progeri eller progeria är en ovanlig sjukdom som gör att kroppen åldras i förtid (geromorfism).Namnet progeri kommer från grekiskan och betyder ungefär gammal i förtid (πρό, pro, före, γῆρας, gēras, ålderdom).Sjukdomen beror på hastig celldöd, som bryter ner cellerna i en alltför snabb takt. Det finns två sorters progeri: Werners syndrom som är den.
  2. Multifunctional enzyme that has both magnesium and ATP-dependent DNA-helicase activity and 3'->5' exonuclease activity towards double-stranded DNA with a 5'-overhang. Has no nuclease activity towards single-stranded DNA or blunt-ended double-stranded DNA. Binds preferentially to DNA substrates containing alternate secondary structures, such as replication forks and Holliday junctions
  3. Werner, Otto synonyms, Werner, Otto pronunciation, Werner, Otto translation, English dictionary definition of Werner, Otto. or Wer·ner's syndrome n. An autosomal recessive disorder characterized by short stature and the appearance of premature aging after puberty, with early..
  4. Pseudo-Cushing's syndrome is a medical condition in which patients display the signs, symptoms, and abnormal hormone levels seen in Cushing's syndrome.However, pseudo-Cushing's syndrome is not caused by a problem with the hypothalamic-pituitary-adrenal axis as Cushing's is; it is mainly an idiopathic condition, however a cushingoid appearance is sometimes linked to excessive alcohol consumption
  5. Parkinsonian syndrome. Polycystic ovary syndrome. Postural orthostatic tachycardia syndrome. Prader-Willi syndrome. Progeria. Progeroid syndromes
  6. Woodhouse-Sakati syndrome. Quite the same Wikipedia. Just better. To install click the Add extension button. That's it. The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time
  7. Werner (comic), comic figure by Rötger Feldmann, called Brösel; Werner (moon crater), named after the astronomer Johannes Werner (3891) Werner, asteroid named after Robert A. Werner; Werner Plan, first attempt to establish the European monetary union; Werner syndrome, autosomal recessive disease; Companies: Werner (Coventry), motorcycle.
Alien Syndrome - C64-Wiki

Wagner Syndrome - EyeWik

symptoms genetic syndromes diagnosis bardet biedl syndrome. Web. Medical Information Search English. English Español Carpal Tunnel Syndrome Antiphospholipid Syndrome Klinefelter Syndrome Porcine Reproductive and Respiratory Syndrome Reye Syndrome Bartter Syndrome Werner Syndrome HELLP Syndrome Ehlers-Danlos Syndrome Brugada Syndrome Bloom. Werner syndrome , also known as adult progeria,[1] is a rare, autosomal recessive disorder[2] which is characterized by the appearance of premature aging.[3] For faster navigation, this Iframe is preloading the Wikiwand page for Werner syndrome Infobox_Disease Name = PAGENAME Caption = DiseasesDB = 14096 ICD10 = ICD9 = ICD9|259.8ICD9|259. Werner-Syndrom. Das Werner-Syndrom, benannt nach dem deutschen Mediziner Otto Werner (1879-1936), ist eine autosomal - rezessive Erkrankung, vor allem mesodermaler Gewebe, die zu einem vorzeitigen, etwa in der Lebensmitte einsetzenden Altern ( Progerie) führt. Es ist ein juveniles segmental progeroides Syndrom und zählt zu den.

ウェルナー症候群 - Wikipedi

Wiedemann-Rautenstrauch syndrome - Wikipedi

Wermer's syndrome synonyms, Wermer's syndrome pronunciation, Wermer's syndrome translation, English dictionary definition of Wermer's syndrome. n. 1. Formation of new tissue. 2. Formation of a neoplasm or neoplasms. American Heritage® Dictionary of the English Language, Fifth Edition. Wermer's syndrome - definition of Wermer's syndrome by The. Werner syndrome ATP-dependent helicase, also known as DNA helicase, RecQ-like type 3, is an enzyme that in humans is encoded by the WRN gene. WRN is a member of the RecQ Helicase family.[5] Helicase enzymes generally unwind and separate double-stranded DNA. These activities are necessary before DNA can be copied in preparation for cell division Wernicke-Korsakoff syndrome (WKS) is a combination of two neurological conditions often blended together. Wernicke's encephalopathy is the initial, acute stage of the syndrome. If the individual recovers from the acute stage, Korsakoff amnesic syndrome, the chronic, long-term stage of WKS results. While there are many symptoms, the most. Atypical Werner syndrome synonyms, Atypical Werner syndrome pronunciation, Atypical Werner syndrome translation, English dictionary definition of Atypical Werner syndrome. or Wer·ner's syndrome n. An autosomal recessive disorder characterized by short stature and the appearance of premature aging after puberty, with early.. 197k Followers, 2,248 Following, 747 Posts - See Instagram photos and videos from Chelsea Werner (@showtimewerner

Bloom Syndrome - Causes, Symptoms, Treatment and Pictures

Werner Syndrome: Background, Pathophysiology, Epidemiolog

Otto Werner synonyms, Otto Werner pronunciation, Otto Werner translation, English dictionary definition of Otto Werner. or Wer·ner's syndrome n. An autosomal recessive disorder characterized by short stature and the appearance of premature aging after puberty, with early.. NORD, a 501(c)(3) organization, is the leading patient advocacy organization dedicated to improving the lives of individuals and families living with rare diseases

Related to Wermer's syndrome: Multiple endocrine neoplasia type 1, MEN1 syndrome MEN 1 An inherited neoplasia syndrome characterised by: parathyroid hyperplasia (95%), pituitary adenoma (10%), pancreatic islet hyperplasia, adenoma or carcinoma, and/or adrenal cortical hyperplasia, adenoma and carcinoid tumours Chelsea Werner. 42,404 likes · 2,234 talking about this. I am a 4X SPECIAL OLYMPICS US CHAMPION & 2 X WORLD CHAMPION @womensbest athlete I hope I can be a role model for those who face challenges..

Two other autosomal recessive disorders caused by defects in DNA repair that disrupt a RECQ helicase are Werner syndrome and Rothmund-T syndrome. As is the case with BSyn, persons with Werner syndrome and Rothmund-T syndrome generally have short stature and DNA instability. Both conditions have clinical features that overlap with. The most widely studied of the progeroid syndromes are Werner syndrome (WS) and Hutchinson-Gilford Progeria Syndrome (HGPS), because they resemble natural aging. [2] Because of its property of accelerated aging (senescence), progeroid syndomes have been widely studied in the fields of aging, regeneration , stem cells and cancer What is Li-Fraumeni Syndrome?The Li-Fraumeni Syndrome (LFS) is a hereditary cancer predisposition syndrome first reported in 1969 by Drs. Frederick Li and Joseph Fraumeni from the National Cancer Institute. What caught their attention was the wide range of cancers found in affected families, the inherited higher risk of developing cancer across several generations, and th

Helicase / The Molecules of Molecular Biology

Looking for Werner? Find out information about Werner. 1. Abraham Gottlieb . 1749--1817, German geologist. He emphasized the importance of field and laboratory observation for understanding the earth 2. Explanation of Werner RAPADILINO syndrome. Quite the same Wikipedia. Just better. To install click the Add extension button. That's it. The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time Wernerin oireyhtymä on erittäin harvinainen oireyhtymä, josta kärsivät ihmiset alkavat vanheta huomattavasti tavallista nopeammin murrosiän jälkeen. Sairauden yleisyydessä on alueellista eroa; Japanissa (arviolta 1/30 000) esiintyvyys on huomattavasti korkeampi kuin esimerkiksi Yhdysvalloissa (arviolta 1/200 000). Oireyhtymä on nimetty saksalaisen Otto Wernerin mukaan, joka kuvasi. CHARGE syndrome is a disorder that affects many areas of the body. CHARGE is an abbreviation for several of the features common in the disorder: coloboma, heart defects, atresia choanae (also known as choanal atresia), growth retardation, genital abnormalities, and ear abnormalities.The pattern of malformations varies among individuals with this disorder, and the multiple health problems can. Berlin Syndrome: Directed by Cate Shortland. With Teresa Palmer, Max Riemelt, Matthias Habich, Emma Bading. A passionate holiday romance leads to an obsessive relationship, when an Australian photojournalist wakes one morning in a Berlin apartment and is unable to leave

베르너 증후군 - 위키백과, 우리 모두의 백과사

felty syndrome. Wikipedia. Medical Information Search. A low white blood cell count usually only occurs in people with Felty's syndrome with an enlarged liver and spleen. The The most common problem is carpal tunnel syndrome caused by compression of the median nerve by swelling around the wrist. Other, rather rare, skin associated symptoms include pyoderma gangrenosum, Sweet's syndrome. The adult version of progeria syndrome is Werner syndrome. The symptoms of Werner syndrome normally occur in teenagers. People with this condition may live into their 40s or 50s Hereditary mixed polyposis syndrome (HMPS) is a hereditary condition that is associated with an increased risk of developing polyps in the digestive tract, most commonly in the colon and/or rectum. A polyp is a growth of normal tissue that forms a lump. As the name suggests, a variety of polyps may occur. People with HMPS are thought to have an. RecQ helikáza je označení pro vysoce konzervovanou rodinu helikáz, které jsou díky své nepostradatelné roli v mnoha procesech souvisejících s DNA považovány za tzv. ochránce genomu, protože se podílí na udržování stability genetické informace a zároveň potlačují vznik nádorového bujení.. Zatímco u bakterií a kvasinek byla identifikována pouze jedna RecQ.

Herlyn-Werner-Wunderlich syndrome Radiology Reference

Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face. Explore symptoms, inheritance, genetics of this condition A surname, from German .· A town in Ontario, Canada.··A male given name from German, equivalent to English Warne Werner Schmid (born February 13, 1930, † January 3, 2002) was a Swiss doctor and geneticist.He was a pioneer in human cytogenetics and a co-founder of the journal Cytogenetic and Genome Research.. Life. Werner Schmid grew up in Winterthur.He studied medicine in Zurich and Paris.After stays abroad in Austin and Houston, he was called back to Zurich in 1962 to set up a cytogenetic laboratory.

Famous birthdays SeptTranslated version of http://derjulian

Werner syndrome - Wiktionar

Lynch syndrome, also known as hereditary non-polyposis colorectal cancer (HNPCC), is a type of inherited cancer syndrome associated with a genetic predisposition to different cancer types. This means people with Lynch syndrome have a higher risk of certain types of cancer. Cancer begins when normal cells begin to change and grow out of control. Ukurasa huu umebadilishwa kwa mara ya mwisho tarehe 15 Aprili 2013, saa 03:27. Maandishi yanapatikana chini ya leseni ya Creative Commons Attribution-ShareAlike License; matakwa mengine yanaweza kutakiwa.Tazama maelezo zaidi ya Matakwa ya Utumiaji.; Sera ya faragh Werner syndrome. Italian. WS. Last Update: 2014-12-09 Usage Frequency: 3 Quality: Reference: Wikipedia Warning: This alignment may be wrong. Please delete it you feel so. English. syndrome werner. Italian. Sindrome di Werner. Last Update: 2014-12-09. Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology. 139 (1): 130-9. Buschke-Ollendorff syndrome, Menkes syndrome, pseudoxanthoma elasticum, and Williams syndrome.Elastosis is the buildup of Cutis laxa Elastic fibers Elastin receptor Resilin: an invertebrate protein Williams syndrome Mithieux, SM; Weiss, AS (2005) Synonyms for Wermer's syndrome in Free Thesaurus. Antonyms for Wermer's syndrome. 2 words related to neoplasia: pathologic process, pathological process. What are synonyms for Wermer's syndrome

Werner syndrome on emaz

HWWS - Herlyn-Werner-Wunderlich Syndrome. Looking for abbreviations of HWWS? It is Herlyn-Werner-Wunderlich Syndrome. Herlyn-Werner-Wunderlich Syndrome listed as HWWS. Herlyn-Werner-Wunderlich Syndrome - How is Herlyn-Werner-Wunderlich Syndrome abbreviated Abstract: Carpal tunnel syndrome (CTS) is the most common nerve entrapment. Electrodiagnostic (EDX) studies are a valid and reliable means of confirming the diagnosis. This monograph addresses the various EDX techniques used to evaluate the median nerve at the wrist