The Guadalajara-Camptodactyly Syndrome-an unusual case

Facial dysmorphism (midfacial hypoplasia, hypertelorism, long neck, small, posteriorly rotated ears) and subnormal intelligence were compatible with Type I variant but muscle (gluteal hypoplasia), genital (labial hypoplasia) and skeletal findings (brachydactyly, simian creases, osteopenia and pelvic...

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Bibliographic Details
Published in:Pediatric Rheumatology 2011-09, Vol.9 (S1), p.P221-P221, Article P221
Main Authors: Khubchandani, RP, Hasija, RP, Dewoolkar, M
Format: Article
Language:English
Subjects:
Pediatrics
Poster Presentation
Rheumatology
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Summary:Facial dysmorphism (midfacial hypoplasia, hypertelorism, long neck, small, posteriorly rotated ears) and subnormal intelligence were compatible with Type I variant but muscle (gluteal hypoplasia), genital (labial hypoplasia) and skeletal findings (brachydactyly, simian creases, osteopenia and pelvic hypoplasia) were seen as has been described in the Type II variant.
ISSN:1546-0096
1546-0096
DOI:10.1186/1546-0096-9-S1-P221