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Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

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

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

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

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

The chapter explains causes of hair loss and excessive hair growth in animals.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

The guide explains how to diagnose and treat hair loss in dogs, covering causes and treatments, with some conditions lacking treatment options.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

New treatments targeting specific genes show promise for treating keratin disorders.

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

Chemokine signaling is important for hair development.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

XEDAR triggers a specific signaling pathway in cells.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Topical Imiquimod may fight vascular tumors by affecting blood vessels or the immune system, low iron might be linked to some hair loss, removing the top skin layer helps vitamin C get in, genetic testing helps diagnose skin conditions, and too much iron could worsen skin inflammation.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Minoxidil does not work to inhibit lysyl hydroxylases in newborn mouse lungs.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Conditioned media from mesenchymal stem cells show promise for tissue repair and disease treatment, but more research is needed on their safety and effectiveness.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Red and infrared light therapy improves hair growth in balding patients.