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A woman had unusual hair growth on one side of her chin without a known cause.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

SLHA can be hard to diagnose and needs teamwork between specialists.

Cantú syndrome may be linked to pituitary adenomas.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

Idiopathic hirsutism is the most common cause, followed by PCOS, and insulin resistance should be checked in patients with acanthosis nigricans.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

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

Hormone imbalance is linked to Hidradenitis Suppurativa, a skin condition, and treatments like anti-androgenic therapy and metformin can help. It's also suggested to check patients for insulin resistance and Polycystic Ovary Syndrome.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.

A woman was diagnosed with Sheehan's syndrome and a rare complication of diabetes insipidus 33 years after symptoms began, improving with hormone therapy.

Boron neutron capture therapy for head and neck cancer can cause side effects like mouth sores and skin irritation, which vary depending on where the treatment is aimed.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Bevacizumab may worsen hypothyroidism, so thyroid function should be monitored during treatment.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A woman got unwanted hair growth on her face from using bimatoprost eyedrops for glaucoma.

Consider Sertoli-Leydig cell tumors in Peutz-Jeghers syndrome patients with adnexal masses.

A rare ovarian tumor caused a postmenopausal woman to develop male-like features, which improved after surgery.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.