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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

A child with a rare scalp condition regrew hair after treatment.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

Trichohyalin may trigger the immune response causing alopecia areata.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

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

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Applying a tretinoin cream can remove hair plugs and treat trichostasis spinulosa.

Trauma can cause fat inflammation and abnormal hair growth.

Trichosporon inkin and Trichosporon mucoides can cause white piedra on scalp hair.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

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

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Alopecia universalis can be an early sign of HIV.