Barth Syndrome

Barth syndrome

Barth syndrome is a rare metabolic and neuromuscular disorder that appears to only affect males.

Barth syndrome
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Barth Syndrome
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Barth syndrome is a rare congenital metabolic and neuromuscular disorder that affects boys. It is passed from mother to son through the sex-linked, or X, chromosome.

Barth syndrome is the common name for 3-methylglutaconic aciduria type II.

Barth syndrome
Costeff optic atrophy syndrome
Dilated cardiomyopathy
Neutropenia
Delayed growth
more related diseases...» ...

The Barth Syndrome Foundation - Support Group
The Barth Syndrome Foundation - Barth Syndrome - Support Group
The Beginning Experience - Support Group
The Beginning Experience - Support Group ...

Barth syndrome
Basal Cell Naevus syndrome see Gorlin syndrome
Bassen-Kornzweig syndrome see Neuroacanthocytosis disorders
Batten disease
BBS see Bardet-Biedl syndrome
Becker MD see Becker Muscular Dystrophy
Becker Muscular Dystrophy ...

Neutropenia associated with phenotypic (observable physical features of an organism, as determined by both genetic makeup and environmental factors) abnormalities: there are some conditions such as Shwachman syndrome and Barth syndrome, ...

See also: Myopathy, Symptom, Infections, Cardiomyopathy, Death