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A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

New genetic mutations causing hair loss were found in a Chinese family.

Rare ovarian tumors can cause increased male hormones in postmenopausal women; surgery is an effective treatment.

Genetic testing for EGFR mutations is crucial in similar cases.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A rare case showed hair regrowth after chemotherapy for thymoma, suggesting a link between alopecia areata and thymoma.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Somatic BHD mutations are rare in Japanese renal tumors.

Nine hair follicle tumors were found in dogs.

PCOS can cause unusual symptoms like late puberty and enlarged clitoris, making diagnosis difficult.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

Postmenopausal women with excess male hormones may have ovarian tumors, and surgery usually cures them.

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

The study suggests fibrosing alopecia in a pattern distribution has distinct features and may vary by race.

Benign epithelial tumors in dogs don't spread or become cancerous.

A woman died from cancer that spread from a long-standing cyst on her abdomen.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

Sebaceous nevus changes with age, and dermoscopy and RCM are effective for diagnosis.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Surgery removed an ovarian tumor, improving her symptoms and normalizing testosterone levels.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

The boy's symptoms suggest a possible new medical condition.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.