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A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Trichorrhexis nodosa causes hair to break easily, often affecting young to middle-aged black women.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

Peripilar keratin casts are a helpful sign for diagnosing traction alopecia.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

Rare ovarian tumors can cause hyperandrogenism, even if imaging appears normal.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

Surgery on a 68-year-old woman with an ovarian tumor led to reduced hirsutism and normal testosterone levels.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

Optical Coherence Tomography has potential in diagnosing hair loss and monitoring blood clotting, and could be improved for deeper tissue observation and better hair loss understanding.

PCOS requires comprehensive, lifelong care addressing both visible and hidden health issues.

A woman with hair loss had a benign sweat duct tumor found during a scalp biopsy.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

A missing mK6irs1 gene causes hair loss in mice.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Alopecia universalis may be linked to Down syndrome due to genes on chromosome 21.

A girl with red hair developed hair-pulling and body image disorders after being bullied for her hair color.

Hair loss from alopecia areata can rarely be caused by dental problems, and treating the dental issue may reverse the hair loss.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Steroid treatment helps preserve hearing in cochlear implant patients.

Early diagnosis and treatment stopped hair loss and improved the condition.

A postmenopausal woman's high testosterone levels and symptoms improved after removing a tumor from her ovary.

Children with alopecia areata often have related health issues like allergies, autoimmune diseases, or mental health conditions.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.