Article Text

PDF

Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth.
  1. R C Shepherd,
  2. D R Goudie,
  3. J L Tolmie
  1. Department of Paediatrics, Inverclyde Royal Hospital, Greenock, Glasgow.

    Abstract

    We report a mother and two of her children, one female and the other male, who have ptosis, hypertelorism, epicanthic folds, downward slanting palpebral fissures, broad nasal bridge, and minor digital anomalies (fig 1); the children had delayed closure of a large anterior fontanelle. All three affected persons were born prematurely.

    Statistics from Altmetric.com

    Request permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.