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BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Experts met to improve care for ichthyosis patients in Spain.

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.

Non-scarring hair loss can be diagnosed with two 4mm punch biopsies, one cut vertically and the other transversely.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

Macrophages are essential for successful skin growth in reconstructive surgery.

Certain skin conditions can indicate insulin resistance and should prompt lifestyle changes and medical treatment to manage underlying health issues.

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.

Immune cells are essential for early hair and skin development and healing.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Scarring after cleft lip and palate surgery is a major issue, and the review looks at ways to manage it.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Caffeine may help hair growth in hereditary hair loss.

Early subungual melanoma might be treated with less aggressive surgery because it invades the skin under the nail more slowly.

Netherton Syndrome can cause severe skin lesions in rare cases.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.