American journal of medical genetics. Part A · 2013
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
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Tatton-Brown Katrina, Murray Anne, Hanks Sandra, Douglas Jenny, Armstrong Ruth, Banka Siddharth, Bird Lynne M, Clericuzio Carol L, Cormier-Daire Valerie, Cushing Tom, Flinter Frances, Jacquemont Marie-Line, Joss Shelagh, Kinning Esther, Lynch Sally Ann, Magee Alex, McConnell Vivienne, Medeira Ana, Ozono Keiichi, Patton Michael, Rankin Julia, Shears Debbie, Simon Marleen, Splitt Miranda, Strenger Volker, Stuurman Kyra, Taylor Clare, Titheradge Hannah, Van Maldergem Lionel, Temple I Karen, Cole Trevor, Seal Sheila, Childhood Overgrowth Consortium, Rahman Nazneen
Аннотация
Weaver syndrome, first described in 1974, is characterized by tall stature, a typical facial appearance, and variable intellectual disability. In 2011, mutations in the histone methyltransferase, EZH2, were shown to cause Weaver syndrome. To date, we have identified 48 individuals with EZH2 mutations. The mutations were primarily missense mutations occurring throughout the gene, with some clustering in the SET domain (12/48). Truncating mutations were uncommon (4/48) and only identified in the final exon, after the SET domain. Through analyses of clinical data and facial photographs of EZH2 mutation-positive individuals, we have shown that the facial features can be subtle and the clinical diagnosis of Weaver syndrome is thus challenging, especially in older individuals. However, tall stature is very common, reported in >90% of affected individuals. Intellectual disability is also common, present in ~80%, but is highly variable and frequently mild. Additional clinical features which may help in stratifying individuals to EZH2 mutation testing include camptodactyly, soft, doughy skin, umbilical hernia, and a low, hoarse cry. Considerable phenotypic overlap between Sotos and Weaver syndromes is also evident. The identification of an EZH2 mutation can therefore provide an objective means of confirming a subtle presentation of Weaver syndrome and/or distinguishing Weaver and Sotos syndromes. As mutation testing becomes increasingly accessible and larger numbers of EZH2 mutation-positive individuals are identified, knowledge of the clinical spectrum and prognostic implications of EZH2 mutations should improve.