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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

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

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

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.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Found new possible treatments for hair loss.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

A new gene, JMJD1C, may affect testosterone levels in men.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

A gene variation is linked to hair thickness in Asians.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Hair diameter and curvature are mostly determined by genetics.

New models predict male pattern baldness better than old ones but still need improvement.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

The study suggests that hypothyroidism may cause alopecia areata.