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

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.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

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.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Some families have a genetic condition where they are born with irregular scalp defects.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Leg hair can be used for eyelash transplants, resulting in fuller lashes with less maintenance.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Finasteride use during early pregnancy may cause limb deformities in babies.

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

Most dogs have hair whorls on their chest and limbs, with shelter dogs and short-haired dogs having more chest whorls.

A newborn girl had a rare case of salivary gland tissue on her chest, which was safely removed.

Teratoma hair is similar to scalp hair but has a rougher surface and lower adhesive force.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

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

Adult earlobe can have a benign cyst that is usually removed by surgery.

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

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

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

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Some extracts from woods and fungi can promote hair growth better than a known hair growth substance.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.