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A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

Androgenetic alopecia is a common genetic and hormonal hair loss affecting many men and women.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

People with androgenetic alopecia (hair loss) may have a higher risk of developing metabolic syndrome.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Diagnosing PCOS in teenage girls is tricky and requires careful evaluation and management.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

HAIR-AN syndrome is common in young women and can be effectively managed with a comprehensive treatment plan.

Androgenetic alopecia is the most common hair loss in females with PCOS in Egypt.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Hair thickness differences help diagnose hair loss severity.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Polycystic ovary syndrome (PCOS) significantly impacts women's emotional well-being and social lives, requiring treatments that include psychological support.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Women with acromegaly often have irregular periods due to hormone imbalances and growth hormone effects.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A rash from semaglutide may be due to propylene glycol, not the drug itself.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

A girl with a rare skin condition improved after one month of treatment with acitretin.