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Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Ruxolitinib helped a patient with alopecia areata regrow hair.

JAK1 inhibitor may effectively treat alopecia areata when TNF-α inhibitors and corticosteroids fail.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

VKHD and sarcoidosis may share a common cause.

A young man had rare serious side effects from an epilepsy drug, leading to stopping the drug.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A new type of rapid hair loss called ADTA usually gets better on its own within 6 months.

A girl inherited excessive body hair from her mother and grandmother.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

PAON shows skin patterns due to genetic mosaicism.

A three-year-old girl survived a rare serious infection caused by BCG vaccination, which improved after treatment with a leprosy drug.

A rare benign scalp tumor in an infant requires surgical removal.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Intralesional steroids effectively treated a young female's scalp nodules without recurrence.

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

A 72-year-old man with sudden taste issues and hair growth was diagnosed with a severe stomach cancer and died within 5 months.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Haplogroup X found in Altaian population supports Amerindian origin.

Satoyoshi syndrome can cause hair loss and other serious health issues, and is hard to diagnose.

Polyacetylene compounds from Panax ginseng may slow hair growth.

A new diagnostic model can help better diagnose and understand Alopecia Areata.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Carbamazepine may cause reversible nail detachment.