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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

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

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The scraggly mutation causes hair loss and skin defects in mice.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

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

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

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.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

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

The fuzzy gene is crucial for controlling hair growth cycles.

A vitamin D receptor mutation causes rickets and affects immune responses.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.