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The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

A golden lion tamarin had Cushing's disease due to a pituitary tumor, leading to its euthanasia.

Longer hair loss leads to more severe CCCA; early treatment and avoiding damaging hairstyles help regrowth.

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Netherton's disease causes multiple hair defects.

Targeting the protein Caveolin-1 might help treat a type of scarring hair loss called Frontal Fibrosing Alopecia.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

The twins' condition is unique and doesn't match any known syndromes.

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

A Persian cat had a rare skin condition that didn't improve with treatment.

Orbital decompression surgery for Graves' orbitopathy caused double vision in 19% of patients, with similar rates for two surgical methods.

Immune privilege collapse in hair follicles may cause permanent hair loss in certain conditions.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

The girl has an inflammatory type of scarring hair loss.

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

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Benign follicular mucinosis involves immune cells attacking hair follicles.

CK15 is not a reliable marker for stem cells in damaged hair follicles from patients with CCCA.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Hair follicle stem cells can become corneal-like cells with the right environment.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

CCL 27 levels are similar in people with and without alopecia areata.

Some people's hair loss is caused by multiple factors, with the most common being a mix of AGA and CCCA.