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The carpenter syndrome phenotype.
Tarhan, Erkan; Oguz, Haldun; Safak, Mustafa Asim; Samim, Erdal.
Afiliación
  • Tarhan E; Ministry of Health, Ankara Training and Research Hospital, Clinic of Otolaryngology, Ankara, Turkey.
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
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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