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A 63-year-old woman's male-like symptoms were caused by a rare testosterone-producing ovarian tumor, treated by removing her ovaries and fallopian tubes.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Two siblings have a rare hair condition caused by a new genetic variant.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Subclinical hypothyroidism in women with PCOS affects thyroid and hormone interactions but not ovary structure.

Renaming frontal fibrosing alopecia to a syndrome could improve diagnosis and treatment.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

PCOS has three subtypes, with 11-oxygenated androgens increasing metabolic risk.

People with blood group O may have a higher risk of developing post-COVID-19 syndrome.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

The woman had a genetic condition causing high cortisol and androgen levels, treatable with dexamethasone.

PCOS affects many young women in KSA, with mild cases being most common.

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

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

A 17-year-old girl has had repeated hair loss since childhood, which can be triggered by infections like COVID-19.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Diagnosing and treating monilethrix is challenging when it occurs with other hair disorders.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A child died from eating hair, causing severe stomach blockages and infection.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

A 15-year-old girl with missed periods was diagnosed with a pituitary disorder and treated with hormones and steroids.

A young woman's rare ovarian tumor was successfully removed, improving her hormonal symptoms.