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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1994 Sep;31(9):707–711. doi: 10.1136/jmg.31.9.707

Mulvihill-Smith syndrome: case report and review.

O Bartsch 1, K D Tympner 1, E Schwinger 1, R J Gorlin 1
PMCID: PMC1050081  PMID: 7815440

Abstract

We report a 20 year old man with short stature, microcephaly, unusual facies, numerous pigmented naevi, hypodontia, immunodeficiency, and a high pitched voice. Tympner et al had assumed that the patient had a new syndrome of "progressive combined immunodeficiency and ectomesodermal dysplasia". We show here that the condition is identical to the Mulvihill-Smith syndrome (McKusick 176690), a progeroid disorder described in four or possibly five sporadic cases to date. We describe his clinical progress up to the age of 20 years. Our patient suffered from severe viral infections, allergic rhinitis and conjunctivitis, delayed puberty, visual loss, modest achievement in high school, and reactive depression. The immunological, facioskeletal, and dental abnormalities are presented in detail.

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Selected References

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