Nevo syndrome.

Abstract

We describe a male patient born to consanguineous parents with a syndrome of tall stature at birth, hypotonia, wrist drop and long spindle shaped fingers. The clinical features are identical to those previously described in three cases from a single family by Nevo et al. (1974: J Med Genet 11: 158-165). Autosomal recessive inheritance is supported by consanguinity in our case. Follow-up at age 3 years demonstrated significant improvement of hypotonia and motor function, and normal cognitive ability.

Cite this paper

@article{Hilderink1995NevoS, title={Nevo syndrome.}, author={Berthold Hilderink and Han G. Brunner}, journal={Clinical dysmorphology}, year={1995}, volume={4 4}, pages={319-23} }