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A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Many displaced schoolchildren in Cameroon are malnourished, with high rates of thinness, stunting, underweight, and deficiencies in iron and protein.

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

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

Some skin medications are safe for pregnant women, but others pose risks or should not be used.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

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

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Different body areas in mice produce different hair types due to interactions between skin layers.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

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

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Some skin medications are safe during pregnancy and breastfeeding, but others can harm the baby and should be avoided.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Calcium and magnesium in hair increase with age and are higher in adult women.

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

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.