Volume 44, Issue 6 pp. 807-812
Article
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Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome

P. Franceschini

Corresponding Author

P. Franceschini

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica Università di Torino, Piazza Polonia 94, 10126 Torino, ItalySearch for more papers by this author
M. P. Vardeu

M. P. Vardeu

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy

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L. Dalforno

L. Dalforno

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy

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F. Signorile

F. Signorile

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy

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D. Franceschini

D. Franceschini

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy

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R. Lala

R. Lala

Divisione di Endrocrinologia Pediatrica, Ospedale Infantile R. Margherita, Torino, Italy

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P. Matarazzo

P. Matarazzo

Divisione di Endrocrinologia Pediatrica, Ospedale Infantile R. Margherita, Torino, Italy

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First published: 1 December 1992
Citations: 19

Abstract

We describe a 3-generation family in which mother, maternal grandfather, and 2 (male and female) children have variably manifestations of the ulnar-mammary syndrome, including ulnar ray defects, obesity, hypogenitalism, delayed puberty, hypoplasia of nipples and apocrine glands, and a previously undescribed ectopia of upper canines. The index patient also had split-hand appearance on the right due to complete absence of the 4th ray. To our knowledge this is the first documented example of split hand in the ulnar-mammary syndrome. The hand anomaly raises the question of a possible causal relationship between ulnar-mammary syndrome and the split hand with aplasia of the ulna syndrome, as already hypothesized by Lenz [1980]. © 1992 Wiley-Liss, Inc.

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