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Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

The document explains various skin conditions in cats and how to diagnose and treat them.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

Long COVID patients may have hormonal imbalances linked to their symptoms.

No single treatment is consistently effective for alopecia areata, and more research is needed.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

The cause of alopecia areata was unknown, and while various treatments existed, no best treatment was agreed upon.

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

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

The new treatment regimen was effective in promoting significant hair growth in all 15 male patients with androgenic alopecia.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

Testosterone helps human pancreatic cells increase insulin release.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

The guideline suggests using specific criteria to diagnose PCOS, recommends various treatments for its symptoms, and advises screening for related health issues.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Children with autoimmune hair loss have similar vitamin D levels to healthy kids, suggesting no extra screening is needed.

The study found no link between vitamin D deficiency and psoriasis but suggests more research is needed.

Low vitamin D levels can cause hair loss and supplements may improve it.

Estrogen therapy can reduce skin aging but has cancer risks.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Secondary amenorrhea has many causes and requires thorough evaluation to treat and restore menstrual cycles.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.