Use this to navigate - Click on a word

Pierre Robin Syndrome

The condition is characterised by a small mandible (jaw bone), lack of tongue control with a high arched or cleft palate. Obstruction of the airway can occur due to the position of the tongue. Associated problems are feeding and breathing difficulties may be severe. However, the jaw continues to grow after birth and the condition improves with age.

Inheritance Patterns:   Most are sporadic events; some cases may be due to Stickler Syndrome which has autosomal dominant inheritance.

Pre-Natal Diagnosis: Where a cleft palate is present it may be able to identify this using ultrasound scanning.

Further information available from:

Mrs Jacqui Mitchell,
Pierre Robin Syndrome Contact group
83 Swallowfield road
London
SE7 7NT
(Tel: 0181 853 1811 evenings)

The Pierre robin contact group is a small Contact group. It offers:

  • Support especially for parents with new babies with the syndrome
  • Support and encouragement for parents with older children

Return to the Medical Index

HOME  :  EVENTS  :   NEWS  :  BUILDING  :  AIMS  :  RESPITE  :   HELP US  :  CONTACT US