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Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Some therapies using stem cells and platelet-rich plasma may help treat osteoarthritis, but more research is needed to ensure they are safe and effective.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

Pannexin 3 is important for bone formation and the development of bone cells.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Inhaling medicine may reduce side effects and improve treatment for a major lung cancer type.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

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

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Trichotillometry is a reliable method to measure hair strength and assess hair loss treatments.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

Rosacea is a skin condition with unclear causes, classified into four subtypes.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

Long COVID causes various long-term health issues and needs better awareness and treatment.

The document concludes that "Dictamnus" has a rich cultural history and potential as a herbal medicine, warranting more research into its effects and safety.

Light microscopy is useful for diagnosing different hair disorders.

Careful planning and patient counseling can lead to excellent hair transplant results, often in one or two sessions.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.

Skin grafting can help repigment vitiligo, but it's less effective for widespread cases due to the Koebner phenomenon.

Oral propranolol successfully treated a baby's skin growth and ulceration linked to PELVIS syndrome.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

Linear skin conditions are rare, more common in females, and often misdiagnosed without tissue analysis.

Most children with skin inflammation taking methotrexate had lab abnormalities, but liver issues often improved without changing the medication dose.

White hair follicles in vitiligo have fewer and less functional melanocytes.

Transplanting skin cells is a safe, effective, and affordable treatment for vitiligo.