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The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Dermoscopy helps diagnose rare GLPLS in males.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

ODC transgenic mice can model human hair loss with skin lesions.

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

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

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

A postmenopausal woman had rare symptoms due to a possible ovarian tumor, needing thorough evaluation.

Sequential therapy with dupilumab and baricitinib improved hair regrowth and atopic dermatitis in a child without adverse reactions.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

An Indian woman with Short Anagen Syndrome had very short hair and a lower quality of life.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

Lichen planopilaris can occur with multiple autoimmune diseases.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

The patient responded well to treatment with no disease progression.

Dupilumab effectively treats various inflammatory skin diseases beyond its initial use for atopic dermatitis.

Nail abnormalities in children can indicate deeper health issues.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

A six-year-old girl has early signs of puberty, needs no treatment, but requires regular check-ups for future health risks.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Sudden hair whitening may be linked to immune system activity.