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A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

Certain genetic variations are linked to hair loss in Mexican men.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Inositol prevents hair loss and improves health in rats.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Infliximab successfully treated a severe hair loss case in Sri Lanka.

KeraGLO improves skin and hair health.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

RIPK1 inhibitors might help prevent alopecia areata.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Acrodermatitis enteropathica can be linked to dental issues, so thorough dental exams are important.

Biotin should be added to Japanese amino acid formula to prevent deficiency.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A Nigerian baby with neonatal lupus got better with treatment by 6 months.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Ruxolitinib helped a patient with alopecia areata regrow hair.

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

Alopecia areata incognito in children can be effectively treated with triamcinolone acetonide and supplements, leading to full hair regrowth.

A unique gene mutation was found in a family with monilethrix.