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

The document concludes that HAIR-AN syndrome should be considered when a patient shows severe hyperandrogenism and insulin resistance after excluding tumors.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Crohn's disease can cause hair loss before other symptoms appear.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A woman with Cushing's syndrome improved after surgery to remove a tumor causing the condition.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The woman's surgery lowered her testosterone and improved scalp hair loss but did not change her excessive body hair.

A woman with inflammatory bowel disease improved after treatment with ustekinumab for a rare skin condition associated with her disease.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Stopping finasteride and closing PFO can help prevent strokes in young adults.

The method creates realistic, anonymous acne face images for research, achieving 97.6% accuracy in classification.

A thorough diagnostic process and teamwork are crucial for managing complex hyperandrogenism in postmenopausal women.

AI is revolutionizing healthcare by improving diagnosis, treatment, and monitoring, but still needs close supervision.

Non-invasive methods can effectively diagnose and manage alopecia areata.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

STIM1 is essential for sweat secretion.

OCT can effectively screen and diagnose various medical conditions non-invasively.

Proretinal nanoparticles are a safe and effective way to deliver retinal to the skin.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Gene mutations can cause problems in male genital development.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

A woman's adrenal tumor disappeared after treatment with cyproterone acetate.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Primary care is key in managing PCOS, focusing on lifestyle changes and medications like birth control and metformin.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.