Lathosterolosis

Alternate names

• Sterol c5-desaturase deficiency
• SC5D deficiency

Summary

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.

Epidemiology

Only 4 cases have been reported in the literature to date.

Cause

Lathosterolosis is due to mutations in the SC5D gene (11q23.3). A mutation in this gene leads to a deficiency in 3-beta-hydroxysteroid-delta-5-desaturase, which is necessary in the conversion of lathosterol into 7-dehydrocholesterol. This prevents the synthesis of cholesterol, which among other functions acts as a structural lipid, a precursor for bile acids and steroid hormones, and is necessary for the maturation of hedgehog morphogens during embryonic development.

Inheritance

Autosomal recessive inheritance, a 25% chance

Lathosterolosis is inherited in an autosomal recessive manner. The parents of an affected child are obligate heterozygotes and they therefore have a 25% chance of having an affected child with each pregnancy.

Signs and symptoms

• Microcephaly is present at birth along with hypotonia, failure to thrive and facial dysmorphic features such as bitemporal narrowing, ptosis, puffy cheeks, and micrognathia.
• Limb anomalies that have been reported include postaxial polydactyly of upper or lower limbs (mainly feet), bilateral syndactyly between the 2nd and 3rd or 2nd and 4th toes and bilateral club feet.
• Developmental delay and learning disability starting in early childhood have been noted in all patients. Additional anomalies have also been reported such as corneal clouding, cataract, conductive hearing loss, gingival hypertrophy, ambiguous genitalia, horseshoe kidney and neurological manifestations (i.e. myoclonus).
• Liver disease seen in patients ranges from hypertransaminasemia to progressive cholestasis and can lead to end stage hepatic disease, occurring in childhood.

Diagnosis

Diagnosis is based on clinical and biochemical findings. An elevation of lathosterol by gas chromatography/mass spectroscopy (GC/MS) is noted in both skin fibroblasts and plasma.

The levels of 7-dehydrocholesterol and cholesterol are normal or low. Molecular genetic testing revealing mutations in the SC5D gene confirms the diagnosis.

Differential diagnosisThe main differential diagnosis is Smith-Lemli-Opitz syndrome that shares many clinical features with lathosterolosis but that can be excluded with biochemical and genetic testing.

Antenatal diagnosisPrenatal diagnosis is feasible if the mutations are known but it has never been performed given the rarity of the disease.

Treatment

Treatment involves cholesterol supplementation and reduction of 7-hydrocholesterol.

Simvastin, a 3-hydroxy-3-methylglutaryl co-enzyme A (HMG-CoA) reductase inhibitor, has been proven to be beneficial in normalizing the lathosterol level in one patient.

Liver transplantation was successful in normalizing liver function and cholesterol levels in a patient who had developed end stage liver disease. Moreover, it appeared to improve neurocognitive functions. Regular opthalmological evalutations and ultrasound monitoring of the liver are recommended.

Prognosis

The prognosis is poor but treatment appears to prolong life and arrest progression of neurological damage.

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NIH genetic and rare disease info

• NIH info on Lathosterolosis

Lathosterolosis is a rare disease.

Lathosterolosis Resources
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