Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Publication year range
1.
Dermatol Online J ; 7(2): 8, 2001 Dec.
Article in English | MEDLINE | ID: mdl-12165224

ABSTRACT

Trichorhinophalangeal syndrome (TRPS) is characterized by its unique facial features and skeletal abnormalities. A bulbous, pear-shaped nose, elongated philtrum, sparse hair, cone-shaped epiphyses and mild growth retardation are found in both type I (TRPSI) and type II (TRPSII). TRPSII can be distinguished from TRPSI when multiple exostoses or redundant skin are present. While TRPSI is inherited in an autosomal dominant fashion, most cases of TRPSII are sporadic although there are a few cases which are familial. The following is a case report of TRPSII with incomplete penetrance in the index case and exostoses and growth retardation in the patient's two siblings.


Subject(s)
Langer-Giedion Syndrome/pathology , Adolescent , Exostoses, Multiple Hereditary/genetics , Exostoses, Multiple Hereditary/pathology , Female , Genes, Dominant/genetics , Hearing Loss, Conductive/pathology , Humans , Langer-Giedion Syndrome/classification , Langer-Giedion Syndrome/surgery
SELECTION OF CITATIONS
SEARCH DETAIL
...