WT limb blood syndrome: Difference between revisions

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(Created page with "__NOTOC__ {{Infobox_Disease | ICD10 = D61.0 | OMIM = 194350| UMLS = C1327917| MeSH = C536751| }} {{SI}} {{CMG}}; {{AE}} {{RT}} ...")
 
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   OMIM          = 194350|
   OMIM          = 194350|
   UMLS          = C1327917|
   UMLS          = C1327917|
   MeSH          = C536751|
   MeshID        = C536751|
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Revision as of 18:17, 2 August 2012

WT limb blood syndrome
ICD-10 D61.0
OMIM 194350
MeSH C536751

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Overview

WT limb-blood syndrome is a rare syndrome characterized by hematological and musculoskeletal anomalies often appearing in childhood.

Historical Perspective

WT limb-blood syndrome is named after two families with surnames starting with W and T, in which multiple members had features characteristic of the disease.

Pathophysiology

Genetics

WT limb-blood syndrome has an autosomal dominant pattern of inheritance.

Associated Conditions

Differentiating from other Disease

WT limb-blood syndrome is differentiated from Fanconi anemia by the autosomal dominant pattern of inheritance and absence of chromosome breakage.

Epidemiology and Demographics

  • The prevalence of this disease is <0.1/100 000.
  • The disease often appears in childhood.

Diagnosis

Physical Examination

Extremities

  • Syndactyly
  • Bifid or hypoplastic thumbs
  • Ulnar and radial defects

References

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