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Biotin treatment can significantly improve hair loss and motor functions in certain metabolic disorders.

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

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.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

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.

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.

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.

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

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Follistatin helps hair growth and cycling, while activin prevents it.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

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

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Dogs could be good models for studying human hair growth and hair loss.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

The study concluded that hair loss in Indian women is not significantly linked to anemia or thyroid problems, but checking thyroid function could help those with ongoing hair loss.

Hair changes can indicate systemic diseases or medication effects.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.