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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A girl with Crohn's disease had a hairball causing bowel obstruction, which was removed, and she recovered well.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Fermented extracts may help hair growth.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

Uncombable hair is inherited dominantly with complete penetrance.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Both penicillamine and tiopronin have significant side effects, but trying the alternative drug can be beneficial if the first is not tolerated.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.

A condition called Central Centrifugal Cicatricial Alopecia causes hair loss and scalp burning in middle-aged African women, and it's treated with various medications, hair transplants, and non-drug methods like wigs.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Early diagnosis and treatment can reduce cicatricial alopecia in middle-aged individuals, especially females.

Celtis choseniana may help treat hair loss by reducing androgen effects and boosting hair growth signals.

A cat had a rare skin disorder with hair loss and scaling, linked to a suspected tumor.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A new gene variant causes curly coats in some dog breeds.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

Chemotherapy often causes temporary hair loss, which is distressing and needs better treatment and support.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Researchers found a non-functional sheep keratin gene due to mutations.

Feline pododermatitis is less common in cats than in dogs.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Ritlecitinib is a new treatment for severe hair loss in people 12 and older.