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A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Certain genes are linked to the risk of developing Alopecia Areata.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Platelet-rich Plasma (PRP) helps treat hair loss effectively, especially when prepared using the double-spin method.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

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

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

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

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

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

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

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

A mother's diet at conception can cause lasting genetic changes in her child.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

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

Dutasteride is the most studied alternative drug for androgenetic alopecia, but more high-quality research is needed.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

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 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 man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

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.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Scientists found a gene in mice that causes early hearing loss.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.