Author(s): Santos, MI ; Beleza-Meireles, A ; Loureiro, S ; Fonseca, M ; Reis, CF ; Rodrigues, F ; Ramos, F ; Ramos, L ; Cardoso, E ; Saraiva, JM
Date: 2013
Persistent ID: http://hdl.handle.net/10400.4/1537
Origin: Repositório do Centro Hospitalar e Universitário de Coimbra
Subject(s): Síndrome de Kabuki
Aims: Although there are more than 400 cases of Kabuki syndrome described in the literature, it is believed that this syndrome is under-diagnosed. Most cases occur sporadically, despite cases with autosomal dominant familial transmission being described. Here we describe three cases identified in the same family. Cases description: A family (mother and two children) was diagnosed with Kabuki syndrome. The three patients show the typical characteristics (facial appearance, musculoskeletal abnormalities, cognitive impairment, growth retardation and peculiar dermatoglyphic pattern) associated with other anomalies described in the syndrome (congenital heart disease and increased susceptibility to infections). Genetic studies revealed a nonsense mutation c.14710 C > T (p.Arg4904X) in the MLL2 gene in the three members of the family. Conclusions: With the description of another case of familial Kabuki syndrome, the authors wish to illustrate the autosomal dominant inheritance with variable expressivity, which are present in this situation, and to alert to the need for a rigorous clinical and molecular evaluation of the affected patient’s relatives, allowing appropriate genetic counseling.
