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

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Alopecia Areata Incognita causes widespread hair thinning, and treatment with systemic corticosteroids and psychiatric support can lead to remission.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.

Haplogroup X found in Altaian population supports Amerindian origin.

Pathologic tissues have more soluble proteins than normal tissues.

Reflectance confocal microscopy reliably identifies skin cancer features like horizontal skin tissue sections.

A new classification system for skin cysts was proposed to improve diagnosis.

Nail disorders not caused by infection are common and can look similar, with psoriasis being the most frequent and having specific nail symptoms.

The document concludes that compulsive hair disorders, like trichotillomania, are complex and require careful diagnosis and treatment from both psychiatric and dermatological perspectives.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Hirsutism involves excessive hair growth due to hormonal issues and can be treated with medication or surgery.

Dermoscopy improves diagnosis of hair and scalp disorders and can help avoid unnecessary biopsies.

The study found a significant link between the renin-angiotensin system and insulin resistance in women with polycystic ovary syndrome.

The document concludes that choosing the right biopsy site is crucial for accurate alopecia diagnosis, and combining methods can improve results.

Early treatment and lifestyle changes are important for managing PCOS in young people to prevent long-term health issues.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Special and immunohistochemical stains are not routinely needed for diagnosing hair disorders.

Almost all patients with chronic kidney disease not yet on dialysis have at least one skin problem.

A small number of premenopausal female blood donors had high prolactin levels, often due to stress, and retesting is recommended to prevent misdiagnosis.

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

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Most patients with telogen effluvium had low iron and vitamin D levels; iron supplements were commonly prescribed.

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

The article suggests renaming Polycystic Ovarian Syndrome (PCOS) to "Hyperandrogenic Persistent Ovulatory Dysfunction Syndrome" (HA-PODS) for accuracy and consistency, but no final decision was made.

Gentle hair care and avoiding harsh treatments can help manage hair loss.