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Boron neutron capture therapy for head and neck cancer can cause side effects like mouth sores and skin irritation, which vary depending on where the treatment is aimed.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

Patients with long COVID after Omicron had fewer hospitalizations and milder symptoms but more fatigue, insomnia, and cough compared to those with Delta.

Vismodegib is effective for basal cell carcinoma but has severe side effects.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The conclusion is that teeth, hair, and claws have similar stem cell niches, which are important for growth and repair, and more research is needed on their regulation and potential markers.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

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

Fungal infection was the main cause of hair loss in Egyptian children studied.

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

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

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

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

A medication called sodium valproate likely caused a girl's hair to become kinky and dry.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.