Article
Molecular and clinical studies in 8 patients with Temple syndrome.
Clinical genetics - 1 Jun 2018
Gillessen-Kaesbach G, Albrecht B, Eggermann T, Elbracht M, Mitter D, Morlot S, van Ravenswaaij-Arts C M A, Schulz S, Strobl-Wildemann G, Buiting K, Beygo J
Abstract excerpt
Temple syndrome (TS14, #616222) is a rare imprinting disorder characterised by phenotypic features including pre- and postnatal growth retardation, muscular hypotonia and feeding difficulties in infancy, early puberty and short stature with small hands and feet and often truncal obesity. It is caused by maternal uniparental disomies, paternal deletions and primary imprinting defects that affect the chromosomal...
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