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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

COVID-19 patients often experience hair loss and scalp pain, which may be related to the severity of their infection and treatment drugs.

Erlotinib causes skin inflammation through IL-1, which can be reduced by anakinra.

Doctors should actively prevent and treat skin side effects in cancer patients to keep them on the best medication and reduce discomfort.

Neomycin is a common cause of follicular contact dermatitis, which is treated by avoiding the allergen and using creams.

Tinea capitis is common in the Eastern Province of Saudi Arabia and can be effectively treated.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Sweat hypersensitivity can cause severe skin issues in horses.

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

The boy's hair loss was due to a hair-pulling disorder, not just a fungal infection.

A man's rash caused by Finasteride improved after stopping the drug and starting new treatments.

Acne necrotica can be effectively treated with topical cream and antibiotics.

During the COVID-19 pandemic in China, skin conditions like eczema and warts increased among children, while respiratory-transmitted skin infections decreased, partly due to mask-wearing.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The woman has a rare, harmless skin condition specific to pregnancy that causes itchy bumps and will go away after she gives birth.

A woman thought to have rosacea was actually suffering from Frontal Fibrosing Alopecia, a hair loss condition. Despite treatment, her condition didn't change, showing the importance of accurate early diagnosis.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Tinea faciei should be considered in neonatal vesicular lesions and confirmed with KOH examination and culture.

COVID-19 may worsen hair loss, but treatments like minoxidil can help.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Hairless protein can block vitamin D activation in skin cells.

Spermidine may help reduce hair loss and deserves further testing as a treatment.

Hydroxychloroquine may help delay skin damage in lupus patients.

Epidermal nevi are skin cell clusters linked to various syndromes.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

Sarcoidosis is more common and severe in Black patients than in Caucasians, requiring early diagnosis and treatment.