| Literature DB >> 7125819 |
L Toudic, G L'Henoret, D Rivière, M L'Hour, Y Castel.
Abstract
A child with the 49 XXXXY syndrome is presented. Diagnosis was possible early in life, because of craniofacial anomalies and congenital cardiac malformations. The main symptoms are growth retardation, craniofacial abnormalities, hypogonadism, frequent bone lesions and severe mental retardation.Entities:
Mesh：
Year: 1982 PMID： 7125819
Source DB: PubMed Journal: Arch Fr Pediatr ISSN： 0003-9764