Telfer Sugar Jaeger syndrome
Alternate names
Piebald trait neurologic defects; White forelock and leukoderma with neurological impairment
Definition
Piebald trait-neurologic defects syndrome is a rare, genetic, pigmentation anomaly of the skin syndrome characterized by ventral as well as dorsal leukoderma of the trunk and a congenital white forelock, in association with cerebellar ataxia, impaired motor coordination, intellectual disability of variable severity and progressive, mild to profound, uni- or bilateral sensorineural hearing loss. There have been no further descriptions in the literature since 1971.
NIH genetic and rare disease info
Telfer Sugar Jaeger syndrome is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - Telfer Sugar Jaeger syndrome
|
Resources
| Additional resources | ||
|---|---|---|
|
Telfer Sugar Jaeger syndrome
|
 | This Telfer Sugar Jaeger syndrome article is a stub. You can help WikiMD by expanding the page. |
<html><link rel="canonical" href="https://wikimd.com/wiki/Telfer+Sugar+Jaeger+syndrome"> <meta name=”viewport” content=”width=device-width, initial-scale=1″> </html>
