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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

Further research is needed to understand lymph node involvement in axillary hidradenitis suppurativa.

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

Cortisone reductase deficiency can cause high androgen and cortisol levels and may be missed in women with similar symptoms.

Elderly patients have more severe hidradenitis suppurativa and may need different treatments.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Early physical exams are crucial for timely Klinefelter syndrome diagnosis.

Leydig cell hyperplasia can cause virilization in postmenopausal women and is treatable with surgery.

Trichostasis spinulosa can look like acne but usually affects adults, not children.

Careful diagnosis is crucial in premature pubarche cases, as 20% have other conditions.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A man developed skin lesions as a side effect of a gamma secretase inhibitor used for treating a tumor.

Hirsutism and acanthosis nigricans are important for diagnosing PCOS; dermatologists play a key role in early detection and treatment.

Improving access to hidradenitis suppurativa care can reduce social disparities.

The first pediatric case of naevus trichilemmocysticus was documented.

Hyperandrogenism is diagnosed using clinical signs, lab tests, and imaging.

Ovarian hemangioma is a rare, benign tumor that can be treated effectively with surgical removal.

Older age is the main risk factor for hemorrhagic cystitis after stem cell transplants.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

Different skin conditions show distinct types of vessel inflammation, a new quality of life index for vulval disease is reliable, a certain intrauterine system might be linked to chronic vaginal yeast infections, and oral minoxidil reduces hair loss in women.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Avoiding exposure to certain grasses can prevent skin allergies, highlighting the importance of proper sanitation.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.