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Article

The FG syndrome: report of a large Italian series.

American journal of medical genetics. Part A - 1 Oct 2006

Battaglia A, Chines C, Carey J C

Abstract excerpt

Initially described as a rare MCA/MR syndrome occurring only in boys, due to a recessive mutation on the X chromosome [Opitz and Kaveggia, 1974], the FG syndrome (FGS) now emerges as a more common disorder also occurring in girls. Based on over 50 reported cases, FGS is associated with developmental delay (especially speech), hypotonia, postnatal onset relative macrocephaly, prominent forehead, frontal hair...

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Identifiers

PMID: 16691600
DOI: 10.1002/ajmg.a.31302

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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