A previously unreported X-linked MCA/MR syndrome is described in 4 members of a large family. Phenotypic manifestations include mental retardation, microcephaly, failure to thrive, severe congenital hypotonia, characteristic face, hypogenitalism, pachygyria. This appears to be an X-linked dominant trait with decreased penetrance and expressivity in carrier females.

Zollino, M., Mastroiacovo, P., Zampino, G., Mariotti, P., Neri, G., New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria, <<AMERICAN JOURNAL OF MEDICAL GENETICS>>, 1992; 43 (1-2): 452-457. [doi:10.1002/ajmg.1320430168] [http://hdl.handle.net/10807/37011]

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria

Zollino, Marcella;Mastroiacovo, Pierpaolo;Zampino, Giuseppe;Mariotti, Paolo;Neri, Giovanni
1992

Abstract

A previously unreported X-linked MCA/MR syndrome is described in 4 members of a large family. Phenotypic manifestations include mental retardation, microcephaly, failure to thrive, severe congenital hypotonia, characteristic face, hypogenitalism, pachygyria. This appears to be an X-linked dominant trait with decreased penetrance and expressivity in carrier females.
1992
Inglese
Zollino, M., Mastroiacovo, P., Zampino, G., Mariotti, P., Neri, G., New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria, <<AMERICAN JOURNAL OF MEDICAL GENETICS>>, 1992; 43 (1-2): 452-457. [doi:10.1002/ajmg.1320430168] [http://hdl.handle.net/10807/37011]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/37011
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