RareTrial

Rare condition

Autosomal recessive primary microcephaly

ORPHA:2512 ↗Gene WARS1Gene SARS1Gene CITGene NUP37Gene NCAPD3Gene CENPEEtiological subtype
Search all Autosomal recessive primary microcephaly trialsAlert me when a trial opens

4

studies recruiting now

as of 7 Sept 2026

35

studies registered in total

as of 7 Sept 2026

4

countries with a recruiting site

as of 7 Sept 2026

28 Jan 2026

most recent study posted

among recruiting studies

Recruiting trials

Showing the 4 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

Search all Autosomal recessive primary microcephaly studies

Where recruiting studies are running

Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.

BelgiumSingaporeSpainUnited States

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Patient organisations

We do not yet list a dedicated organisation for this condition. The directories below are the best route.

NORD ↗GARD ↗Orphanet ORPHA:2512 ↗

About Autosomal recessive primary microcephaly

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (WARS1, SARS1, CIT, NUP37, NCAPD3, CENPE).

Orphanet expert page ↗GARD (NIH) ↗

Related conditions

Autosomal recessive chorioretinopathy-microcephaly syndrome

Renal

Autosomal Recessive Polycystic Kidney Disease

Autosomal recessive cerebral atrophy

Autosomal recessive Alport syndrome

Autosomal recessive multiple pterygium syndrome

Neurological

Autosomal recessive spastic ataxia of Charlevoix-Saguenay

Connective Tissue

Autosomal recessive spondylocostal dysostosis

Neurological

Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia

Blood

Congenital autosomal recessive small-platelet thrombocytopenia

Neurological

Adult-onset autosomal recessive cerebellar ataxia

Neurological

Autosomal recessive ataxia due to PEX10 deficiency

Neurological

Autosomal recessive ataxia due to ubiquinone deficiency

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).