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The document does not determine if adults with aphallia are fertile.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.

Intense Pulse Light effectively reduces hair growth in faun tail nevus.

Microneedling with betamethasone led to almost complete hair regrowth in severe alopecia areata.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The book provides an overview of new trends and techniques in cosmetic dermatology.

Different types of alopecia in children require specific diagnoses and treatments.

A teenage girl with a fungal scalp infection got better with antifungal and allergy medication, and special shampoo.

A woman's hair loss was caused by her husband's testosterone gel and a diabetic man's nail disease led to bone infection, both treated successfully.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Use "female pattern hair loss" term, assess androgen excess, treat with minoxidil and other medications if needed.

The conclusion is that published guidelines are improving transgender medical care, but more research and education in transgender medicine are needed.

Progesterone treatment improved seizures in a woman with menstrual cycle-related epilepsy, but a wrong medication worsened her condition.

Neuroimaging suggests that treatments targeting brain steroids could help control epilepsy, especially types linked to the menstrual cycle.

Testosterone therapy seems safe and effective for transgender men with proper care, but more long-term research is needed.

A woman's severe skin reaction was caused by an allergy to a skin treatment.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

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

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

Researchers found a gene mutation responsible for a rare hair loss condition.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Monkeys with hair loss during pregnancy showed higher stress hormone levels and invested differently in their offspring.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.