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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Scientists can now create skin with hair by reprogramming cells in wounds.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A specific gene mutation causes Olmsted syndrome.

Hirsutism is mainly caused by high androgen levels or sensitivity, with PCOS being the most common cause.

Hair restoration follows a specific pattern.

A special receptor in sensory nerve endings helps control how they respond to stretching.

A patient grew extra hair on their ears after treatment for testicular cancer, possibly due to hormonal changes or genetics.

Lupus treatment requires a combination of drugs and therapies, with research needed for new options.

A cat with ear infection and skin issues was successfully treated for Demodex mites using imidacloprid and moxidectin.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Celiac disease can cause skin problems that may get better with a gluten-free diet.

African baobab fruit is a good source of antioxidants and micronutrients, but too much can cause laxative effects.

Psychiatrists are crucial in pain management teams because they help treat severe pain and related mental health issues.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The review found that PRP is the most effective treatment for hair loss with few side effects.

PRP treatment can increase hair growth in male pattern baldness, but this effect is not linked to the levels of growth factors or the number of platelets.

Cantú syndrome is caused by mutations in the ABCC9 gene.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Cattle skin has leptin which might control skin and hair growth.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.