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Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

People with alopecia areata often have lower iron levels than healthy people.

Children with autoimmune hair loss have similar vitamin D levels to healthy kids, suggesting no extra screening is needed.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Check serum ferritin levels and total blood count for women with diffuse hair loss.

Preventing zinc deficiency is crucial, especially in bowel disease and chronic malabsorption, with recommended skin checks and zinc supplements.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Treatment with 5α-reductase inhibitors is linked to a delay in prostate cancer diagnosis and may affect survival rates.

Vitamin D deficiency is common in children with non-scarring alopecia, and managing it may help treatment.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Men with early balding showed higher levels of certain genes linked to hair loss and possibly prostate cancer.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Vitamin B12 deficiency can cause reversible hair color loss in children.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Valproic acid treatment increases a specific acid in urine by blocking an enzyme, possibly causing skin rash and hair loss.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Low ferritin and high Anti TPO levels are linked to early hair greying.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Low vitamin D and ferritin levels are linked to female hair loss.

Four-amino acid part makes enzyme sensitive to finasteride.

Iron supplements can restore normal hair color in cases of premature graying linked to iron deficiency.