Disorders

Jawad Syndrome

Synonym(s): Microcephaly with Mental Retardation and Digital Anomalies

Gene	Locus	Protein
RBBP8	18q11.2	DNA endonuclease RBBP8

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.