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The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

PCOS is a common hormonal disorder in women that can be managed with lifestyle changes and various medications.

Insulin resistance and high male hormone levels are major causes of Polycystic Ovary Syndrome.

The conclusion is that proper diagnosis and long-term treatment, including medication, hair removal, and lifestyle changes, are important for improving hirsutism, especially in PCOS patients.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

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 emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

PRP helps hair growth in common hair loss disorder.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Gene linked to common hair loss found, may lead to new treatments.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

New treatments for skin conditions in children include a preferred drug for birthmark reduction, proactive creams for eczema and vitiligo, a safe psoriasis medication, and special tissues and socks for eczema and fungal infections.

Different problems with hair stem cell renewal can lead to hair loss.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

The study found that Short Anagen Syndrome results in short hair growth not due to hair fragility, and hair may grow longer after puberty.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

Diagnosing oral ulcers can be complex and requires careful examination and follow-up.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

Skin symptoms can indicate endocrine disorders and have various treatments.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.