Lathosterolosis

MONDO:0011816

Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease.

Also known as: lathosterolosis, sterol C5-desaturase deficiency, Sc5D deficiency

41 clinical trials for this condition and its sub-types.

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