Brain calcification, Rajab type
A rare inherited disorder characterized by widespread calcifications of basal ganglia and cortex developmental delay small stature retinopathy and microcephaly. The absence of progressive deterioration of the neurological functions is characteristic of the disease.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version February 2024
Newly diagnosed with
Brain calcification, Rajab type?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
To fund research for treatment and/or a cure for CASK Gene Disorder
For a list of clinical trials in this disease area, please click here.