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[XXXXY syndrome].

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.

Authors

, , , ,

Source

Archives francaises de pediatrie 39:4 1982 Apr pg 247-9

MeSH

Abnormalities, Multiple
Heart Defects, Congenital
Humans
Hypogonadism
Infant
Intellectual Disability
Male
Sex Chromatin
Sex Chromosome Aberrations

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

fre

PubMed ID

7125819

Citation

Toudic, L, et al. "[XXXXY Syndrome]." Archives Francaises De Pediatrie, vol. 39, no. 4, 1982, pp. 247-9.
Toudic L, L'Henoret G, Rivière D, et al. [XXXXY syndrome]. Arch Fr Pediatr. 1982;39(4):247-9.
Toudic, L., L'Henoret, G., Rivière, D., L'Hour, M., & Castel, Y. (1982). [XXXXY syndrome]. Archives Francaises De Pediatrie, 39(4), pp. 247-9.
Toudic L, et al. [XXXXY Syndrome]. Arch Fr Pediatr. 1982;39(4):247-9. PubMed PMID: 7125819.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [XXXXY syndrome]. AU - Toudic,L, AU - L'Henoret,G, AU - Rivière,D, AU - L'Hour,M, AU - Castel,Y, PY - 1982/4/1/pubmed PY - 1982/4/1/medline PY - 1982/4/1/entrez SP - 247 EP - 9 JF - Archives francaises de pediatrie JO - Arch. Fr. Pediatr. VL - 39 IS - 4 N2 - 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. SN - 0003-9764 UR - https://www.unboundmedicine.com/medline/citation/7125819/[XXXXY_syndrome]_ DB - PRIME DP - Unbound Medicine ER -