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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Premature hair graying in the face may be influenced by genetics and environment.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

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

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A boy had a rare scalp condition with thickened skin and different-colored hair.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Early diagnosis and comprehensive management improve life quality for Netherton syndrome patients.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Hepatitis C and alcohol abuse may lead to porphyria cutanea tarda.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Early diagnosis and multidisciplinary care are crucial for improving the quality of life in patients with ectodermal dysplasia.

Two siblings both had a rare case of alopecia areata at the same time.

FGF13 gene changes cause excessive hair growth in a rare condition.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.