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Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Zinc is effective for treating various skin conditions, including warts and acne.

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

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

The document concludes that early diagnosis and treatment of PCOS in teenagers is important for managing symptoms and preventing long-term health problems.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Over half of young people in Saudi Arabia experience early gray hair, linked to factors like smoking, stress, and family history.

Blocking interferon-gamma might help treat various autoimmune diseases.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Advances in genetics may lead to targeted treatments for hair disorders.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Biotin supplements significantly improved a young girl's uncombable hair.