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The research linked PLCD1 gene variants to the development of trichilemmal cysts.

PCOS is a common inherited condition causing cysts, irregular periods, and increased diabetes risk in women.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

Eruptive vellus hair cysts are often missed in diagnoses.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

Foals can have various skin issues, some genetic, immune-related, or due to infections and allergies.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Oral isotretinoin was recommended for a 21-year-old woman with severe acne.

Skin cysts might help advance stem cell treatments to repair skin.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

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

The Hairless gene is crucial for healthy skin and hair growth.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Recent progress has been made in understanding inherited hair and nail disorders.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.