Sensorineural deafness, abnormal genitalia, synostosis of metacarpals and metatarsals 4 and 5, and mental retardation: description of a second patient and exclusion …

J Mendioroz, J Fernández‐Toral… - American Journal of …, 2005 - Wiley Online Library
J Mendioroz, J Fernández‐Toral, E Suárez, F López‐Grondona, KW Kjaer, E Bermejo…
American Journal of Medical Genetics Part A, 2005Wiley Online Library
Abstract In 1988 Pfeiffer and Kapferer reported on a patient with sensorineural deafness,
psychomotor delay, hypospadias, cerebral manifestations, and bilateral synostosis of the 4th
and 5th metacarpals and metatarsals. Synostosis of the 4th and 5th metacarpals and
metatarsals is a very rare defect that has been described as an isolated Mendelian defect,
as part of multiple congenital anomaly (MCA) patterns, and in different syndromes. Among a
total of 2,023,155 liveborn infants in the Spanish Collaborative Study of Congenital …
Abstract
In 1988 Pfeiffer and Kapferer reported on a patient with sensorineural deafness, psychomotor delay, hypospadias, cerebral manifestations, and bilateral synostosis of the 4th and 5th metacarpals and metatarsals. Synostosis of the 4th and 5th metacarpals and metatarsals is a very rare defect that has been described as an isolated Mendelian defect, as part of multiple congenital anomaly (MCA) patterns, and in different syndromes. Among a total of 2,023,155 liveborn infants in the Spanish Collaborative Study of Congenital Malformations (ECEMC), we observed only two cases with this type of metacarpal fusion, for a frequency of 1/1,011,577. One had the isolated defect, and the other one that we are describing here, had an MCA pattern similar to that described by Pfeiffer and Kapferer [1988]. We tested HOXD13 but did not find any mutations in exons and intron–exon boundaries. To our knowledge this case is the second one reported with this syndrome. © 2005 Wiley‐Liss, Inc.
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