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Men with early balding may have hormonal imbalances similar to women with PCOS and could benefit from similar treatments.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

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

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Sheehan's syndrome can sometimes cause psychosis.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

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.

A circulating inhibitor caused insulin resistance, but clomiphene improved symptoms.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Some conditions mimic PCOS symptoms and need careful diagnosis to treat potentially serious health issues.

Polycystic ovaries and early male baldness are inherited traits.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Improved nutrition quickly healed the patient's skin lesions.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

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

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

PCOS starts in adolescence with hormonal issues, leading to adult health problems, and early treatment is crucial.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Netherton's syndrome can cause frequent bacterial infections beyond just skin issues.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.