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Studying rare genetic disorders can help us understand and treat common diseases better.

Certain gene variations may increase the risk of hair loss in Egyptians.

Polycystic ovary syndrome is a complex condition that affects women's mental, reproductive, and metabolic health throughout their lives.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Researchers found two new genetic variants linked to Alzheimer's disease.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Some medicinal plants can help heal wounds and may lead to new treatments.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Hepatitis C virus can cause skin diseases and dermatologists play a crucial role in identifying these conditions.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

The new microrhizotron tool effectively observes and measures pepper plant roots non-destructively.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Androgens play a key role in hair growth and disorders like baldness and excessive hairiness.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Toxoplasma gondii infection may increase testosterone levels in males.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Taking vitamin D might improve life for MS patients and reduce skin side effects from alemtuzumab treatment.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Some drugs can cause serious side effects like heart issues and nervous system problems, but certain drugs for Parkinson's and overactive bladder may be safer, though they still have some common side effects.