The carpenter syndrome phenotype.
Int J Pediatr Otorhinolaryngol
; 68(3): 353-7, 2004 Mar.
Article
en En
| MEDLINE
| ID: mdl-15129947
Carpenter syndrome (Acrocephalopolysyndactyly type II), first described in 1901, consists of acrocephaly, syndactyly, polydactyly, congenital heart disease, mental retardation, hypogenitalism, cryptorchidism, obesity, umbilical hernia and bony abnormalities. We report a 6 years old boy presenting as a union of these malformations and also having bilateral sensorineural hearing loss. Auditory disturbances are not common among Carpenter syndrome patients. According to our knowledge, this is the first Carpenter syndrome case whose hearing loss is demonstrated by auditory brainstem response (ABR) test.
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Bases de datos:
MEDLINE
Asunto principal:
Acrocefalosindactilia
/
Pérdida Auditiva Sensorineural
Límite:
Child
/
Humans
/
Male
Idioma:
En
Revista:
Int J Pediatr Otorhinolaryngol
Año:
2004
Tipo del documento:
Article
País de afiliación:
Turquía