Abstract
We report on 2 sibs with generalized hypotonia, developmental retardation, unilateral radio-ulnar synostosis, and a characteristic facial appearance. We propose that they have a new autosomal recessive syndrome.
MeSH terms
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Child
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Dermatoglyphics
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Developmental Disabilities / genetics
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Face / abnormalities
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Female
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Genes, Recessive
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Humans
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Male
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Muscle Hypotonia / genetics
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Phenotype
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Radius / abnormalities*
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Syndrome
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Synostosis / genetics*
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Ulna / abnormalities*