Literature DB >> 20358618

Further delineation of the Kapur-Toriello syndrome.

Nathaniel H Robin1, Katherine D Rutledge, Peter D Ray, John H Grant.   

Abstract

The Kapur-Toriello syndrome (KTS) is a rare multiple congenital anomaly syndrome, with presumed autosomal recessive inheritance based on the initial report of affected siblings. Here we report on a female with multiple anomalies, including cleft lip and palate, coloboma, mental retardation with cerebral atrophy, and imperforate anus who, upon re-evaluation at 30 months, was recognized to have a columella that extended below the nares. This distinctive finding prompted the diagnosis of KTS. This is the 5th report of KTS, and the second female. Interestingly, both female cases also manifest an ano/rectal malformation, suggesting that this should be considered a component manifestation of this rare syndrome. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20358618     DOI: 10.1002/ajmg.a.33349

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Coloboma and anorectal malformations: a rare association with important clinical implications.

Authors:  Giulia Brisighelli; Andrea Bischoff; Marc Levitt; Jennifer Hall; Elizabeth Monti; Alberto Peña
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

2.  Achiasma and Kapur-Toriello syndrome: Two rare entities.

Authors:  Grant A Justin; Keith E Earley; Justin G Peacock; Aaron D Grant
Journal:  Am J Ophthalmol Case Rep       Date:  2019-06-05
  2 in total

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