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People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

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

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

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.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

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.

Fungal infection was the main cause of hair loss in Egyptian children studied.

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.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

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

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

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

Edar signaling is crucial for proper hair follicle development and function.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Progress has been made in skin and nerve regeneration, but more research is needed to improve methods and ensure safety.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

The gene Prss53 affects hair shape and bone development in rabbits.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

The document concludes that while significant progress has been made in understanding skin biology and stem cells, more research is needed to fully understand their interactions with their environment.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

The most common skin problems in Indian children are infections and eczemas.

The skin is the largest organ, protecting the body, regulating temperature, and producing hormones.