Daentl Towsend Siegel syndrome
|Daentl Towsend Siegel syndrome|
|Classification and external resources|
Daentl Towsend Siegel syndrome is a very rare disorder characterized by blue sclerae, kidney malfunction, thin skin, and hydrocephalus. It was first identified by D.L. Daentl et al. in 1978. Daentl Towsend Siegel syndrome is also known as "Hydrocephalus blue sclera nephropathy" and "Familial nephrosis, hydrocephalus, thin skin, blue sclerae syndrome".
- "Familial nephrosis, hydrocephalus, thin skin, blue sclerae syndrome: clinical, structural and biochemical studies.". Birth defects original article series 14 (6B): 315–339. 1978.
- "Daentl Towsend Siegel syndrome (Supplementary Concept)". Medical Subject Headings. Retrieved 2012-08-21.
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