Clin Dysmorphol. 1995 Oct;4(4):347-51.

Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome.

Philip N, Andrac L, Moncla A, Sigaudy S, Zanon N, Lena G, Choux M.

Source

Department of Medical Genetics, Hôpital d'Enfants de la Timone, Marseille, France.

Abstract

We describe a 19-year-old boy who presented with facial dysmorphism, multiple lateral meningoceles, skeletal abnormalities and normal intelligence. Neurofibromatosis and Marfan syndrome were excluded. Electron microscopy of the skin showed non-specific abnormalities suggesting a connective tissue disorder. The features of this boy closely resemble those in a mother and daughter with Lehman syndrome.

PMID:: 8574426; [PubMed - indexed for MEDLINE]

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