Search for a rare disease
Other search option(s)
Isolated congenital microcephaly
Disease definition
A rare neurological disorder characterized by a reduced head circumference at birth with no gross anomalies of brain structure. It can be an isolated finding or it can be associated with seizures, developmental delay, intellectual disability, balance disturbances, hearing loss or vision problems.
ORPHA:199642
Classification level: Disorder- Synonym(s): -
- Prevalence: -
- Inheritance: -
- Age of onset: Antenatal, Neonatal
- ICD-10: Q02
- OMIM: -
- UMLS: C0025958
- MeSH: -
- GARD: 3603
- MedDRA: 10027534
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.