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Antiandrogens affect androgen-dependent body functions and are used for various medical conditions, with some risks like fetus feminization, but new forms like 17α-propylmesterolone show promise for acne without systemic effects.

Some African American women's central scalp hair loss is linked to genetics and past fungal scalp infections, with more research needed on other causes.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Blood tests confirmed a baby in the womb had a CMV infection.

A girl had rickets due to a gene mutation affecting vitamin D response.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

The document concludes that supportive home environments and addressing parent-child interactions can effectively treat trichotillomania in children.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A specific gene mutation causes congenital hair loss.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Men generally face more severe COVID-19 outcomes than women, partly due to hormonal differences.

Most pregnant women experience skin changes like darkening and itching, while serious skin conditions are rare but need early treatment.

Inner city teens had high retention rates for the contraceptive implant, especially those with a history of abortion.

Family members of North Indian women with PCOS have a high rate of metabolic syndrome.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

Topical minoxidil successfully treated temporal triangular alopecia.

Zinc supplements and weaning cured a breast-fed baby's zinc deficiency caused by a gene mutation.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Pregnancy can cause various skin changes, including pigmentation, acne, and stretch marks, and may affect preexisting skin conditions.

Metformin helps manage PCOS by improving fertility and is safe for pregnancy, especially when combined with certain treatments.

Women who had bariatric surgery risk nutritional deficiencies causing skin issues during pregnancy and breastfeeding.

PRP may improve fertility treatment success but needs more research for safe use.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.