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Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

Zinc supplements and diet changes can effectively treat zinc deficiency and prevent complications.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Alopecia areata involves specific T-cells, unlike androgenetic alopecia.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

A woman's hair loss was initially misdiagnosed as scarring hair loss but was actually a treatable autoimmune hair loss.

People with autism are more likely to develop alopecia areata than those without autism.

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

The patient had a severe itchy rash and hair loss in the armpits.

Ritlecitinib effectively treats alopecia areata in patients 12 and older with fewer side effects.

Two siblings both had a rare case of alopecia areata at the same time.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

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

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Researchers found two new genetic variants linked to Alzheimer's disease.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

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

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.