Acampomelic Form of Campomelic Dysplasia with SOX9 Missense Mutation.


Autoria(s): Gopakumar H.; Superti-Furga A.; Unger S.; Scherer G.; Rajiv P.K.; Nampoothiri S.
Data(s)

2014

Resumo

Campomelic dysplasia is a skeletal dysplasia characterized by flat face, Pierre Robin sequence, shortening and bowing of long bones and club feet. The authors describe a case of "acampomelic" campomelic dysplasia that differs from classical campomelic dysplasia by the absence of bone bowing. This condition is among the most common skeletal dysplasias but is often misdiagnosed in the absence of overt campomelia.

Identificador

http://serval.unil.ch/?id=serval:BIB_D60C135BCF00

isbn:0973-7693 (Electronic)

pmid:23564514

doi:10.1007/s12098-013-1007-x

isiid:000329254000019

Idioma(s)

en

Fonte

Indian Journal of Pediatrics, vol. 81, no. 1, pp. 98-100

Tipo

info:eu-repo/semantics/article

article