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Recent progress has been made in understanding inherited hair and nail disorders.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

The skin issues in the two dogs might be caused by infection or self-injury, not genetics.

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

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

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

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

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

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

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

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

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

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.

Older skin has higher cancer risk due to inflammation and stem cell issues.

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

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

Understanding fetal skin development helps diagnose congenital skin diseases.

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

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

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

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

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

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.