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People on immune-modifying skin disease treatments may have a weaker antibody response to COVID-19 vaccines but often improve after the second dose.

Hair loss in alopecia areata can negatively affect sexual quality of life.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Gut bacteria pathways may help treat hair loss in obese people.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

The coronal approach is effective and safe for reducing eye bulging in Graves' eye disease.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Cantú syndrome may be linked to pituitary adenomas.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

A rare pituitary tumor in an 18-year-old male caused hormonal issues and vision loss, requiring surgery and further treatment.

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

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

The patient's long-term symptoms were due to Sheehan's syndrome, which improved with hormone therapy.

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

Treatment restored normal sexual characteristics and blood condition in a patient with testicular cancer.

A 31-year-old woman was diagnosed with Complete Androgen Insensitivity Syndrome much later than usual, leading to a call for earlier detection and treatment guidelines.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

An 8-year-old boy's early puberty was caused by a rare hormone-secreting brain tumor, which was successfully treated with surgery.

Early physical exams are crucial for timely Klinefelter syndrome diagnosis.