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[Turner Syndrome: what's new in medical care?].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 Dec 2011

Zenaty D, Laurent M, Carel J C, Léger J

Abstract excerpt

Turner syndrome is a rare genetic disorder, affecting approximately one in 2500 live-born female, due to total or partial absence of the X chromosome. Typical clinical features are short stature and premature ovarian failure and less constantly phenotypic particularities such as congenital malformations, acquired cardiovascular, otological (hearing impairment), autoimmune and metabolic pathologies. The phenotype...

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Identifiers

PMID: 22041596
DOI: 10.1016/j.arcped.2011.09.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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