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A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Polycystic ovarian disease symptoms can continue after menopause, making diagnosis and management in older women challenging.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Skin problems are common in lupus, often appearing first, with various types and treatments, and careful monitoring is important for diagnosis and management.

Hair loss without scarring is more common than permanent hair loss with scarring, and is often due to genetic factors.

Traditional Chinese Medicine, combined with antiandrogen therapy, could improve treatment and reduce side effects for genetic hair loss.

The document concludes that understanding nail anatomy is key for diagnosing nail diseases, early signs of nail melanoma may allow for less aggressive treatment, and specific genetic mutations are important in thyroid cancer prognosis and treatment.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair disease research is a growing and evolving field in dermatology, with recent significant advances.

Teen hair loss is common, can be caused by genetics or health issues, and can be diagnosed and treated.

Female pattern hair loss in women is caused by hormones and genetics, leading to hair thinning, with various treatments available.

The conclusion is that a systematic approach is key for treating symmetrical alopecia in dogs, but treatment may not always be necessary.

Different hair loss types need accurate diagnosis for proper treatment.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

The book provides updated knowledge on hair disorders and new treatments for hair loss.

The book is a comprehensive and current guide on hair disorders, with minor flaws.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Different factors help diagnose and treat hair loss accurately.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Alopecia areata is caused by the immune system attacking hair follicles.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.