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The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

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

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

New treatments for PCOS focus on managing symptoms and improving fertility.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

The document concludes that systemic autoimmune diseases are complex, incurable, and require ongoing treatment and research.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Vitiligo causes white skin patches and can lead to psychological stress.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

The paper concludes that breast cancer treatment involves complex interactions between medical symptoms, patient experiences, and commercial influences, requiring a holistic approach.

The document concludes that alopecia areata is an unpredictable autoimmune hair loss condition with no cure, but various treatments exist that require personalized approaches.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Hair growth dysfunction involves various conditions with limited treatment options.

A mother and her two daughters got a skin infection from their cat.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

A 22-year-old man has alopecia areata, an autoimmune hair loss condition, with various treatments available.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Eating healthy, exercising, and certain nutrients like myoinositol and omega-3s can help manage PCOS symptoms.

Alopecia areata is a hair loss condition that may be linked to stress and genetics, often requires psychological support, and has no set treatment.