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A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Toxic epidermal necrolysis is a severe skin reaction often linked to drugs, requiring careful medication use and supportive care.

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

Assessing newborn scalp hair can reveal important health information.

Removing vitamin D and calcium receptors in mice skin cells slows down skin wound healing.

Yellow and orange colors are important for diagnosing certain skin conditions.

Some skin diseases and their treatments can negatively affect male fertility.

Male pattern baldness is an unintended side effect of the body's use of androgens for muscle growth, especially in those genetically prone to it.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document explains how shampoos clean, rinses condition, one-step shampoos offer convenience, and hair growth promoters aim to prevent hair loss, emphasizing the importance of scientific evidence for their effectiveness.

FGF9 helps hair follicles grow in small-tailed Han sheep by affecting cell growth and certain signaling pathways.

Sorafenib is effective in treating Desmoid Tumor/Deep Fibromatosis.

Skin symptoms are important for diagnosing infections in children.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

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

Skin fat plays a key role in immune defense and healing beyond just storing energy.

PRP shows promise for improving facial wrinkles, skin elasticity, and hair growth, but more research is needed to standardize its use and understand its effects.