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

A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A woman's sudden hair loss three years after a bone marrow transplant was a sign of chronic graft-versus-host disease but improved with treatment.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

People with allergies or high eosinophil levels have a higher chance of severe hair loss from alopecia areata, and sudden hair loss can indicate chronic graft-versus-host disease.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Recognizing and treating overlap syndrome in connective tissue diseases is crucial.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A new DSG4 gene mutation causes hair defects in a young girl.

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

Anti-Ku antibodies are linked to unique symptoms and may involve autophagy issues.

Late-onset alopecia areata in Taiwanese patients is more common in women, usually starts at age 57, often involves less than 10% hair loss, and may have a minimal link to thyroid issues.

A woman with lupus and severe nerve damage improved with specific treatments.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Low-sulfur hair syndrome can cause UVB sensitivity and testicular failure.

Some multiple sclerosis treatments may trigger hair loss conditions like alopecia areata.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Alopecia universalis from alemtuzumab in multiple sclerosis can be reversed with specific treatments.

Genetic marker rs12558842 strongly linked to male hair loss.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

Misdiagnosis of LPP in AGA patients can cause hair transplant issues.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Androgenetic alopecia worsens with age in Japanese men.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.