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MENT could be a better option than testosterone for male hormone therapy and birth control because it works well at lower doses and has fewer side effects on the prostate.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

The combination treatment showed a higher response rate but no significant survival benefits.

Neuromyotonia and morphoea can occur together in the same body areas.

Nevus comedonicus can sometimes grow terminal hair, challenging previous beliefs.

MG53 helps reduce skin damage caused by nitrogen mustard.

A rare ovarian tumor caused high testosterone in a postmenopausal woman, resolved by surgery.

It's important to consider genetic hair disorders when diagnosing hair loss.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

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

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Trichoblastomas may mimic fetal skin development by having many Merkel cells, unlike adult skin.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Increasing m6A levels can improve skin cell growth and wound healing.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A woman with type 2 diabetes developed alopecia areata, suggesting a link between the two autoimmune conditions.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Monilethrix causes fragile, patchy hair loss.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.