Author/Editor     D'Adamo, Patrizia; Fassone, Lucia; Gedeon, Agi; Janssen, Emiel A
Title     The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
Type     članek
Source     Am J Hum Genet
Vol. and No.     Letnik 61, št. 4
Publication year     1997
Volume     str. 862-7
Language     eng
Abstract     Barth syndrome (BTHS) is an X-linked disorder characterized clinically by the associated features of cardiac and skeletal myopathy, short stature, and neutropenia. The clinical manifestations of the disease are, in general, quite variable, but cardiac failure as a consequence of cardiac dilatation and hypertrophy is a constant finding and is the most common cause of death in the first months of life. X-linked cardiomyopathies with clinical manifestations similar to BTHS have been reported, and it has been proposed that they may be allelic. We have recently identified the gene responsible for BTHS, in one of the Xq28 genes, G4.5. In this paper we report the sequence analysis of 11 additional familial cases: 8 were diagnosed as possibly affected with BTHS, and 3 were affected with X-linked dilated cardiomyopathies. Mutations in the G4.5 gene were found in nine of the patients analyzed. The molecular studies have linked together what were formerly considered different conditions and have shown that the G4.5 gene is responsible for BTHS (OMIM 302060), X-linked endocardial fibroelastosis (OMIM 305300), and severe X-linked cardiomyopathy (OMIM 300069). Our results also suggest that very severe phenotypes may be associated with null mutations in the gene, whereas mutations in alternative portions or missense mutations may give a less severe phenotype.
Descriptors     POINT MUTATION
TRANSCRIPTION FACTORS
X CHROMOSOME
ABNORMALITIES, MULTIPLE
ALLELES
AMINO ACID SEQUENCE
ANIMALS
BASE SEQUENCE
CAENORHABDITIS ELEGANS
CAUSE OF DEATH
CHROMOSOME MAPPING
CONSERVED SEQUENCE
INFANT
INFANT, NEWBORN
MOLECULAR SEQUENCE DATA
NUCLEAR FAMILY
PEDIGREE
PROTEINS
SACCHAROMYCES CEREVISIAE
SEQUENCE ALIGNMENT
SEQUENCE HOMOLOGY, AMINO ACID
SYNDROME