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A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Hypertrichosis causes excessive hair growth and needs psychological support due to its impact on self-esteem.

FGF13 gene changes cause excessive hair growth in a rare condition.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The document concludes that accurate diagnosis and appropriate management are crucial for treating various hair disorders, which have significant psychological impacts.

Cantú syndrome may be linked to pituitary adenomas.

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

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

The conclusion is that managing androgen excess requires long-term treatment, including hormonal contraceptives and androgen blockers, with follow-up after six months.

Various treatments, including FDA-approved drugs, natural products, and oral supplements, can help with hair loss, but a patient's medical history and potential allergies should be considered when choosing a treatment.

PCOS is a long-term condition that needs more research for better understanding and treatment.

A girl inherited excessive body hair from her mother and grandmother.

Hair changes can indicate systemic diseases or medication effects.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

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

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

Cantú syndrome is caused by mutations in the ABCC9 gene.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.