Search

everythinglearnresearchcommunity

for

Search:↓

The case emphasizes the need for careful screening in children for insulin resistance and related conditions.

Dupilumab can improve both atopic dermatitis and alopecia universalis.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

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.

Hidradenitis suppurativa improves with antiandrogen therapy.

Recurrent vaginal bleeding in young girls without puberty signs may require a genital exam to find hidden causes.

Early diagnosis of GLPLS is crucial to prevent complications, but scarring alopecia is irreversible.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

The document concludes that careful planning and execution of facial gender affirmation surgery after at least 12 months of hormonal therapy can improve the quality of life for transgender individuals.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Keratin proteins are consistent across different hair types from the same person.

White piedra is a rare hair infection treated with oral and topical antifungals.

The normal human prostate does not significantly affect blood DHT levels.

Hair loss can happen after severe H1N1 flu but usually grows back in 4 months.

Behavior therapy and medications, especially clomipramine, can help reduce hair pulling in people with trichotillomania.

Hodgkin's lymphoma can show up as hair loss.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

The patient responded well to treatment with no disease progression.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Doctors are preparing to potentially perform uterus transplants in transgender women, considering technical, hormonal, and ethical factors.

The document concludes that proper diagnosis and tailored long-term treatment can effectively manage androgenic disorders in women, improving patient care outcomes.

Early diagnosis and treatment with Leuprolide are key for children with precocious puberty.

Nonshaven follicular unit extraction is a good hair transplant option that doesn't require shaving and can transplant up to 3000 grafts daily.

The study concluded that combination therapy with topical corticosteroids and hydroxychloroquine or finasteride is effective in treating Frontal fibrosing alopecia in Asians.

Rural Bangladeshi girls mature later than peers in other low and middle-income countries due to poor nutrition and socioeconomic conditions.

Hair follicle size is mainly influenced by the number of cells and extracellular matrix volume, with cell number having a larger impact.