Search

everythinglearnresearchcommunity

for

Search:↓

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

Steroid cell tumors in the ovary are rare, can produce testosterone causing symptoms, and are mainly treated with surgery.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Keloids on the penis are rare, often triggered by circumcision, and rarely recur after surgery.

Finasteride effectively treats male hair loss, improving growth and density.

Men with X-linked recessive ichthyosis often experience male-pattern baldness.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

New genes and pathways are important for testosterone production and male sexual development.

Patients with metabolic syndrome had lower Gleason scores when diagnosed with prostate cancer.

An elderly man had a rare, large skin cyst on his lower back, which was removed by surgery.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Middle-aged men with unusual hot flashes should be checked for pituitary tumors.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Male infertility and genitourinary birth defects are often linked to genetic issues.

A female Rottweiler had a rare genetic condition causing mostly hairless skin.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Unilateral keratosis follicularis squamosa may be a new subtype, successfully treated with asiaticoside ointment.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

A 20-year-old woman was found to have a rare ovarian tumor causing symptoms like acne and a low-pitched voice, which disappeared after the tumor was removed.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

Finger length ratios might predict risk for skin condition in males.