Down syndrome

Pre-referral guidelines for primary care providers

Down syndrome is a genetic abnormality characterised by trisomy 21 (95%), with the remaining 5% being due to translocations. It occurs in 1 per 600-800 births in Australia.

Diagnosis

The diagnosis of Down syndrome is often made by antenatal screening. When this has not occurred, it can usually be diagnosed based on the typical phenotypic features present in the newborn including:

  • up-slanting palpebral fissures
  • epicanthic folds
  • flat facial profile
  • low-set small ears
  • open mouth with protruding tongue
  • short neck with increased nape skin
  • short broad hands with incurved 5th finger (clinodactyly) & transverse palmar crease
  • space between first and second toes
  • hypotonia

Rapid confirmation of the diagnosis is possible with a FISH for trisomy 21 followed by a full karyotype to detect Down syndrome due to translocations.

Practice points

  • Diagnosis of Down syndrome is generally made by either antenatal screening or genetic testing in a newborn with typical dysmorphic features.
  • The medical management of a child with Down syndrome is centred around surveillance for common associated health issues and anticipatory guidance for families - see RCH General Medicine, Screening for Children with Down Syndrome.

Management

Medical management is centred around surveillance for common health issues and anticipatory guidance for families - see RCH General Medicine, Screening for Children with Down Syndrome.

There are many associations with Down syndrome which need to be considered, including:

Referral pathways