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Distinct facial appearance with nasal hypoplasia, constipation, severe mental retardation and hypotonia in two unrelated young males
Author(s) -
Fryns JeanPierre,
Troch Chantal De,
Mol Christine Van,
Vandenbossche Luc
Publication year - 1996
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1996.tb02628.x
Subject(s) - hypotonia , medicine , hypoplasia , constipation , pediatrics
In this report we describe two unrelated young males with severe mental retardation, persisting hypotonia, and constipation. A maternal uncle of one of these two boys died at the age of 18 months and presented the same clinical symptoms. The triad mental retardation, hypotonia, constipation is a characteristic finding in the FG syndrome, an X‐linked mental retardation syndrome. At the present time, there is increasing evidence that the FG syndrome‐phenotype may be present in different XLMR conditions, e.g. the fragile X syndrome. In addition to the triad severe mental retardation, hypotonia, constipation, the present two male index patients had a characteristic facial appearance with nasal hypoplasia, relative microcephaly and pre‐and postnatal overgrowth. The question is raised whether the present two males are examples of a specific entity within the FG‐syndrome‐like phenotype.

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