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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Tranexamic acid effectively reduced swelling episodes in a girl with a rare form of hereditary angioneurotic edema.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Hair loss discovery causes stress; talking to dermatologists helps.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

Homeopathy may help with hair loss caused by various factors, especially during the pandemic.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Dermal papilla cells play a key role in hair loss by responding to androgens.

Using minoxidil on the scalp can help grow hair for people with hereditary baldness.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

A new mutation in the HR gene causes hair loss in a specific family.

Microneedling combined with other treatments significantly improves hair growth in people with hair loss and is safe.

Botulinum toxin treatment improves hair follicle width and length in androgenetic alopecia.

Caffeine may help hair growth in hereditary hair loss.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Hair loss in women is often due to hereditary conditions or stress, and while treatments like minoxidil can help, diagnosis and management require medical guidance.

Male androgenetic alopecia (MAA) is a common, hereditary hair loss condition in men, linked to heart disease, and can be treated with minoxidil, finasteride, or hair transplantation.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

A boy with a rare skin condition improved quickly after starting zinc supplements.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

HDMHG0401-10 treatment significantly improved hair count and was better than a placebo in reducing hair loss in men with hereditary hair loss, with no major side effects.

Fat stem cell treatment is safe and increases hair density for hair loss, but more research is needed.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.