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A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Toxic Shock Syndrome progresses quickly, often involves multiple organs, and is linked to Staphylococcus aureus toxins, with treatment options available but diagnostic challenges remaining.

Sarcoidosis can cause severe high calcium levels, hair loss, and kidney failure.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

Finasteride and dutasteride can cause severe, lasting side effects.

The structured oral exam format is effective and well-received for teaching internal medicine.

The book provides a clear overview of PCOD and is recommended for medical trainees and clinicians, but may lack depth for advanced researchers.

Aging affects hair density and skin health, and Behcet's disease, a complex condition with no specific test, involves sores and systemic issues, treated with various medications.

Children with systemic lupus erythematosus have different skin symptoms than adults.

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

Ayurvedic treatment helped a woman with PCOS become pregnant and have a healthy baby.

Diagnosing and treating PCOS is complex due to differing criteria and requires a team approach.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Losing 5-10% body weight can improve PCOS symptoms, letrozole is better than clomiphene for fertility, and managing weight and blood sugar is important to reduce pregnancy complications.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

The document recommends a team-based approach and personalized care for managing diabetes in teenagers.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

Late onset SLE has different symptoms and antibody profiles compared to young onset SLE.

The machine learning model accurately predicts Systemic Lupus Erythematosus in Omani patients.

Most lupus patients in the study experienced hair loss, which greatly affected their mental and social well-being.

Skin issues are common and important for diagnosing PCOS.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The case shows skin changes can indicate deeper health issues like insulin resistance, which are challenging to manage.

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