Abstract
We report on three further cases of mildly retarded patients with marfanoid habitus and a pattern of minor anomalies. These patients are likely to be affected with the Lujan-Fryns syndrome. We have reviewed twenty cases from the literature for a better delineation of this newly recognized disorder.
MeSH terms
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Abnormalities, Multiple / genetics
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Abnormalities, Multiple / pathology*
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Adolescent
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Arm / abnormalities
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Facial Bones / abnormalities
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Foot Deformities, Congenital / pathology
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Genetic Linkage*
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Growth Disorders / pathology*
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Hand Deformities, Congenital / pathology
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Humans
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Intellectual Disability / genetics*
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Male
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Marfan Syndrome
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Skull / abnormalities
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Syndrome
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X Chromosome*