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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The rash on the infant indicated a serious underlying condition.

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

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

A new mouse mutation causes skin and hair defects due to a gene change.

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

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

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

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

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

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

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

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

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

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

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

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.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.