Clark-Baraitser syndrome: report of a new case and review of the literature
- PMID: 15930902
Clark-Baraitser syndrome: report of a new case and review of the literature
Abstract
We describe the case of a boy with moderate mental retardation associated with tall stature, obesity, macrocephaly and typical facial features, characterized by a large 'square' forehead, prominent supraorbital ridges, broad nasal tip, prominent lower lip and minor dental anomalies. We think that our proband is affected by Clark-Baraitser syndrome, a rare X-linked mental retardation disorder, to date described only in five male subjects. We present a more complete definition of the clinical phenotype of the syndrome with particular attention to the behavioural aspect that, in combination with the body size and the dysmorphic picture, we think is distinctive for the Clark-Baraitser syndrome. We also summarize the mild features described in female relatives of the patients, as it could disclose a possible carrier condition and be of help with genetic counselling in the families with male patients, until a molecular test is available.
References
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- Baraitser M, Reardon W, Vijeratnam S 1995. Nonspecific X-linked mental retardation with macrocephaly and obesity: a further family. Am J Med Genet 57:380–384.
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- Clark RB, Baraitser M 1987. Letter to editor: A new X-linked mental retardation syndrome. Am J Med Genet 26:13–15.
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- De Pina-Neto JM, de Molfetta GA 1998. The X-Linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case. Clin Dysmorphol 7:233–234.
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- Reynolds JF 1987. Editor's note: A new X-linked mental retardation syndrome. Am J Med Genet 26:13–15.
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