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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Using CD123 to detect certain immune cells helps diagnose a type of hair loss condition.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

The paper suggests improving diagnosis and treatment of telogen effluvium but does not recommend a new classification system.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Hair can indicate early signs of metabolic disorders, with issues like protein deficiency stopping hair growth.

Changing the diagnosis criteria for PCOS might miss women at risk for related health issues.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

Overweight women with PCOS have higher levels of certain hormones that could indicate a higher risk of heart and metabolic problems.

Eating pacu-manteiga fish can cause Haff disease, leading to severe muscle damage.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

The document concludes that systemic autoimmune diseases are complex, incurable, and require ongoing treatment and research.

The document says PCOS is a common hormonal disorder in women, diagnosed by certain criteria, and managed with lifestyle changes and various medications.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Fungal infection was the main cause of hair loss in Egyptian children studied.

The document concludes that managing PCOS involves treating symptoms and reducing long-term metabolic risks, with lifestyle changes being important.

Mild thyroid issues don't affect the metabolism and hormones of women with PCOS.

The research suggests that p63 and TGF-β1 may help determine tumor type and malignancy in hair follicle and sebaceous tumors.

A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

T-cell reconstitution after thymus transplantation can cause hair whitening and loss.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.

Dermoscopy helps dermatologists diagnose different types of hair loss accurately without always needing a biopsy.

Researchers found four genes that could help diagnose severe alopecia areata early.

Pharmacists should interpret lab data and perform physical exams to improve patient care.