Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0033377 (prolapse)
11,717 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A case of congenital familial ptosis with simultaneous Ehlers-Danlos syndrome type II is presented. Since coincidence of these two rare hereditary diseases would be unlikely, the ptosis in this case may be a so far undocumented manifestation of EDS.
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PMID:[Can familial Eyelid ptosis be an expression of Ehlers-Danlos syndrome?]. 398 3