Literature DB >> 15129947

The carpenter syndrome phenotype.

Erkan Tarhan1, Haldun Oğuz, Mustafa Asim Safak, Erdal Samim.   

Abstract

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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Year:  2004        PMID: 15129947     DOI: 10.1016/j.ijporl.2003.10.009

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  2 in total

Review 1.  Sudden death in a child with Carpenter Syndrome. Case report and literature review.

Authors:  Jeanette M Ramos; Gregory J Davis; John C Hunsaker; M Gregory Balko
Journal:  Forensic Sci Med Pathol       Date:  2009-11-19       Impact factor: 2.007

2.  Multifaceted Functions of Rab23 on Primary Cilium-Mediated and Hedgehog Signaling-Mediated Cerebellar Granule Cell Proliferation.

Authors:  C H H Hor; J C W Lo; A L S Cham; W Y Leong; E L K Goh
Journal:  J Neurosci       Date:  2021-07-01       Impact factor: 6.167

  2 in total

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