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A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A new gene mutation linked to a skin condition was found in a Spanish family.

New genetic mutations linked to rare skin disorders were found in three newborns.

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

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

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

A specific mutation in PA-PLA1α causes abnormal hair growth.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

Hair examination helps diagnose rare neurological diseases in children.

Hair loss in certain mice is linked to changes in keratin-related genes.