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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

A new method using visual aids to diagnose hair diseases was effective after brief training.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Removing the liver tumor improved the patient's skin condition and hair growth.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

A woman was wrongly diagnosed with lupus but actually had leprosy.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Exclamation-mark hairs and yellow dots indicate alopecia areata, while follicular ostia loss and white scarring indicate lichen planopilaris and discoid lupus erythematosus.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Finding eosinophils near hair bulbs helps diagnose alopecia areata.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

New mutations in the hairless gene may cause hair loss and affect bone development.

Syphilitic alopecia is a rare hair loss condition in secondary syphilis that looks similar to another condition but can be diagnosed with specific tests and responds to antibiotics.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The four patients have a unique type of ichthyosis affecting hair follicles.

The same gene mutation can cause different symptoms in family members.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

White hair regrowth in alopecia areata may be more common than thought.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

A rare dual diagnosis of alopecia areata and lichen planopilaris requires thorough evaluation for effective treatment.