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A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Light/laser therapy can effectively increase hair density in some types of alopecia, especially androgenic alopecia and alopecia areata.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

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

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

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

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

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

The document concludes that accurate diagnosis and management of PCOS are crucial due to its associated health risks.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The conclusion is that accurately identifying the cause of high androgen levels in women with PCOS is crucial and requires specific tests.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Thyroid hormones affect skin texture, hair and nail growth, and can cause skin diseases related to thyroid problems.

Finasteride may help reduce tic severity in male Tourette syndrome patients.