POSTNATAL SECTION

This section processes approximately 5,500 blood samples per year from, babies, children and adults. The laboratory offers high resolution karyotyping supported by additional Molecular Cytogenetic (FISH) studies when appropriate.
The major referral categories are:
Paediatric referrals:
Congenital abnormalities/ dysmorphism, learning difficulties including ? Fragile X syndrome, developmental delay, atypical sexual development, short stature, features suggestive of a specific syndrome and confirmation of prenatal diagnosis

Adult referrals:
Infertility, Recurrent pregnancy loss (3 or more), family history of a chromosome abnormality and learning difficulties.

For sample requirements and guidance on reporting times, click here

Available downloads:
Cytogenetics referral form

Author: Gareth Masson Authorised by: Graham Fews Version 1.0.1.1
Authorised on 13/01/2010 Next review date 13/06/2011
ONLY VALID ON DAY OF PRINTING