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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.

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

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

Cantú syndrome may be linked to pituitary adenomas.

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.

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

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.

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

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

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

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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.

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

The document is a detailed medical reference on skin and genetic disorders.

Too much androgen can cause hair loss; finasteride may help.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Androgens, like DHT, affect hair growth and treatments like finasteride may help.

FGF12 is important for hair growth and could be targeted for hair loss treatment.

Hair changes can indicate systemic diseases or medication effects.

Valproic acid can cause hair loss when taken orally but may promote hair growth when applied topically.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

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.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."