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Early hair loss may predict heart disease.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

5% minoxidil works better for hair growth and density, with minor irritation.

TGF-β signaling is crucial for stem cell maintenance, differentiation, and has implications for cancer treatment.

Systemic Lupus Erythematosus has varied symptoms and is hard to diagnose, affecting many body parts and requiring careful clinical judgment.

Women generally handle heart enlargement better than men, but it's riskier for them if it occurs; hormones like estrogen offer some protection.

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

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

The lecture concluded that drugs for human enhancement are here to stay and called for their responsible development and fair access.

Follicular Unit Transplantation is a precise hair restoration technique that requires careful planning and a skilled team, and Follicular Unit Extraction offers a less invasive option.

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.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The document suggests using natural remedies like bloodletting and honey for various health issues but lacks scientific evidence for their effectiveness.

Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

Dermatologists can help detect and manage eating disorders by recognizing skin changes.

DHEA may help with sexual function when used intravaginally by menopausal women but is similar to hormone therapy in other aspects and might cause more side effects like acne and hair loss.

Early recognition and management of connective tissue diseases like lupus are crucial in young patients.

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.