38 top medical experts on Lathosterolosis across 3 countries and 3 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Lathosterolosis: 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: 3-beta-hydroxysteroid-delta(5)-desaturase deficiency, Deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase, Sterol C5-Desaturase Deficiency
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