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A 17-year-old girl had severe, on-and-off hair loss, likely due to COVID-19. She was treated with Vitamin D3, biotin, and other supplements, and saw some improvement within a month.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

KFSD causes scarring hair loss and skin roughness, mainly in males.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Treating early puberty with hormone therapy may increase the risk of polycystic ovary syndrome in adults.

Reflectance confocal microscopy helped tell periorificial dermatitis apart from similar skin conditions.

Most rural children with scalp ringworm had a non-inflammatory type and early treatment is important to prevent complications.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

Fascial Manipulation treatment helped a woman with vulvodynia and other health issues.

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

Adding colchicine stopped the girl's recurring heart issues caused by lupus.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The document summarizes important skin care topics for non-specialist doctors, including treatments for skin conditions and the management of skin diseases.

Habit reversal training effectively treats hair-pulling disorder in both adults and children.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

The document discusses how to identify and manage common skin conditions in children.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

A 7-year-old boy's unusual hair loss was caused by a herpes infection and healed after treatment.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Hair loss can be treated with medications like minoxidil and finasteride or surgery, but treatment effectiveness varies by alopecia type and accurate diagnosis is important.

Girls with PCOS often start puberty earlier and have signs of insulin resistance from a young age.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Polycystic ovaries are defined by having 12 or more small follicles in each ovary and are found in up to 33% of women, while Polycystic Ovary Syndrome (PCOS) is the most common hormone disorder in women of reproductive age, potentially increasing risk of obesity, diabetes, and heart diseases.