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Frontal fibrosing alopecia is linked to increased immune system activity and reduced stem cells, suggesting early treatment targeting this pathway might prevent hair follicle damage.

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

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The document concludes that doctors should monitor children's brain development when treating hemangiomas with interferon alfa and consider stopping the treatment if problems arise, while also exploring drugs that might counteract side effects.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

PC-associated alopecia has unique microscopic features.

Gloriosa superba poisoning can mimic severe tropical infections and cause rapid hair loss.

A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

A woman survived a massive lithium overdose that caused a form of hair loss.

Two new gene mutations cause a rare hair disorder.

Hair diameter difference, brown skin discoloration around hair follicles, and missing hair in certain areas are key signs of androgenetic alopecia (commonly known as hair loss) when viewed under a dermoscope.

Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Infectious cerebral vasculitis can be a severe complication of meningoencephalitis, regardless of the pathogen.

Researchers found a new mutation causing total hair loss from birth.

The document concludes that human astrocytes aid stroke recovery, research confidence affects student career aspirations, collagen affects cancer spread, a microRNA suppresses brain cancer growth, calmodulin regulates water channels, and small magnesium pieces deform differently.

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

A unique type of hair loss mimics another condition but has minimal inflammation and specific immune cells present.

CTE can distort results in hair growth trials, so exclude it carefully.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

A woman's hair loss from graft versus host disease helps understand similar hair loss conditions.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

New mutations in the DSG4 gene cause a rare hair condition.

A 16-year-old boy's alopecia areata progressed unusually to resemble male pattern baldness.

The patient's hair has unique structural differences with alternating bright and dark bands.