Microcephaly-congenital cataract-psoriasiform dermatitis syndrome

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Microcephaly-congenital cataract-psoriasiform dermatitis syndrome

Synonyms: SMO deficiency | Sterol-C4-methyl oxidase deficiency

A rare sterol biosynthesis disorder characterized by microcephaly bilateral congenital cataract mild developmental delay growth delay with short stature psoriasiform dermatitis of variable severity and immune dysregulation. Behavioral disorder joint contractures and arthralgia have also been described.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024

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Advocacy Organizations

Genetic Support Network of Victoria

The Genetic Support Network of Victoria is an organisation that supports people living with genetic, undiagnosed and rare conditions and those who support them including community and families, patient support organisations, health professionals and industry. Our vision is our community flourishing and living their best lives.

Mississippi Metabolics Foundation

Our mission at Mississippi Metabolics Foundation (MMF) is to advocate, educate, and support families in MS affected by genetic metabolic disorders/inborn errors of metabolism (IEM's). MMF promotes initiatives and further advancements in legislation, education, research, clinical trials, studies, therapies, targeted treatments, and eventual cures for IEM’s and all rare diseases.

Clinical Trials

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