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

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Patients often experience long-lasting changes to their hair after stem cell transplants.

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

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Hair loss needs more research for better treatments.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

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

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

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

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

Women with excessive male-pattern hair growth should get a full hormone check-up to find and treat any underlying issues, considering both medical and emotional aspects.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Effective hirsutism management requires identifying the cause, combining new and traditional treatments, and setting realistic expectations for patients.

A new mutation in the HR gene causes hair loss in a specific family.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.