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

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

Epidermal stem cells could lead to new treatments for skin and hair disorders.

Androgens play a key role in hair growth and disorders like baldness and excessive hairiness.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Neurohormones help control skin health and could treat skin disorders.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

Melanocyte development from neural crest cells is complex and influenced by many factors, and better understanding could help treat skin disorders.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

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.

Dermal papilla cells are key for hair growth and color, influencing hair type and size, and their interaction with stem cells could help treat hair loss and color disorders.

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.

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

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

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

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

Scientists created stem cells that can grow hair and skin.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.