Search

everythinglearnresearchcommunity

for

Search:↓

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A boy's hair turned red because of genetic mutations, not lack of zinc.

A woman with high testosterone and an adrenal nodule had an ovarian tumor causing her symptoms, which improved after the tumor was removed.

A rare ovarian tumor can occur without causing male-like symptoms.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

Certain gene changes and hormone levels are linked to female hair loss.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Severe CCCA may be biologically and clinically different from milder forms.

Giant pituitary macroadenomas causing Cushing disease are rare and may need extra treatment if surgery fails.

The baby's hair loss was due to congenital syphilis, which was treated with penicillin.

Genetic testing can identify causes of rare hair loss disorders in children, but no treatments exist.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by affecting androgen functions and suppressing certain hormones.

Mohamed Kandil suggests renaming Polycystic Ovary Syndrome to "Polyfollicular Anovulatory Androgenic Syndrome" to better describe its symptoms, but concerns exist that it may not cover all related issues like obesity and depression.

A 6-year-old Asian boy has a rare scalp condition causing hair loss and thickening, with unclear causes and no effective treatment.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

FOXN1 duplication can cause excessive hair growth.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Hirsutism and acanthosis nigricans are reliable skin signs of PCOS and suggest the need for further tests for related health issues.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

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 family had a genetic condition causing hair loss on the scalp, passed down through four generations.