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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.

Knocking out certain genes in mice helps understand skin and hair growth problems.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

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

Understanding skin structure and development helps diagnose and treat skin disorders.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

A20 protein is crucial for normal skin and hair development.

Chemokine signaling is important for hair development.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

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.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Light microscopy is useful for diagnosing different hair disorders.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Hair changes can indicate systemic diseases or medication effects.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

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.