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A woman recovered from hair loss and skin eruptions after stopping a tuberculosis drug and using steroids.

The study found a specific pattern of uneven melanin distribution on balding scalps that could help understand skin diseases caused by light exposure.

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

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Non-invasive imaging helped diagnose a woman's severe hormone imbalance and diabetes, and medication successfully treated her condition.

The document discusses challenges in eye care, including treating melanoma before macular hole repair, bloody tears resolved by blood pressure control, eyelash regrowth in hair-pulling disorder with medication, a non-invasive method to detect eyelash mites, and the psychological factors affecting contact lens comfort.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

Using a special laser and skin medication together successfully cleared a skin condition in a pregnant woman.

Topical ruxolitinib quickly improves non-segmental vitiligo.

Melanocytes can regenerate around hair follicles in bullous pemphigoid, especially in patients with darker skin.

Home IPL devices safely and effectively reduce hair and prevent pilonidal disease recurrence.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

Hyperandrogenism is a common hormonal disorder in women, often linked to PCOS.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

Several treatments are effective for pigmentary disorders like vitiligo and melasma.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

β-interferon injections for melanoma can cause excessive hair growth at the injection sites.

Early diagnosis and comprehensive care are crucial for managing Focal Dermal Hypoplasia's complex symptoms.

Patients with acanthosis nigricans often have insulin resistance and signs of increased male hormones, but treatment targeting these male hormones is generally ineffective.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

HAIR-AN syndrome is common in young women and can be effectively managed with a comprehensive treatment plan.

Segmental vitiligo affects hair follicle melanocytes, causing small, uniform depigmented spots.

Estrogens and progesterone are key in regulating melasma pigmentation.