Short stature, sensorineural deafness, ocular abnormalities and severe mental retardation in two siblings. A new syndrome?

Clin Dysmorphol. 2004 Jul;13(3):173-177. doi: 10.1097/01.mcd.0000115200.74297.cf.

Abstract

We describe a brother and sister with craniofacial dysmorphism, short stature, relative obesity, sensorineural deafness, multiple pigmented naevi and severe mental retardation. One sibling had keratoconus and the other had an iris coloboma. Dysmorphic features included brachycephaly, hypotelorism, small mouth, thin lips, pterygium colli, broad chest, widely spaced nipples and cutaneous second and third toe syndactyly. The children demonstrate some features of Noonan syndrome, but we believe that they have a different and distinctive phenotype. We have reviewed similar cases in the literature and discuss these in the context of our cases, who may have a previously undescribed syndrome.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Adolescent
  • Adult
  • Body Height
  • Brain / abnormalities
  • Coloboma / complications
  • Coloboma / diagnosis
  • Diagnosis, Differential
  • Eye Abnormalities / complications
  • Eye Abnormalities / diagnosis*
  • Eye Abnormalities / genetics
  • Facies
  • Family Health
  • Female
  • Hearing Loss, Sensorineural / complications
  • Hearing Loss, Sensorineural / diagnosis*
  • Hearing Loss, Sensorineural / genetics
  • Humans
  • Intellectual Disability / complications
  • Intellectual Disability / diagnosis*
  • Intellectual Disability / genetics
  • Keratoconus / complications
  • Keratoconus / diagnosis
  • Male
  • Noonan Syndrome / diagnosis
  • Phenotype
  • Syndactyly / diagnosis
  • Syndrome