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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

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

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Lack of cystatin M/E causes thin hair and dry skin.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Non-ablative and ablative fractional lasers helped hair growth in some cases without major side effects, but didn't work for all hair disorders.

Mutations in the KRT85 gene cause hair and nail problems.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Bimatoprost is safe and improves eyelash growth in healthy kids but not in those with eyelash loss from chemotherapy or alopecia.

Skin symptoms like fragile skin and easy bruising can indicate Cushing's syndrome, which requires early diagnosis and treatment to prevent serious health issues.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

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

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

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

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Woolly hair is a rare genetic condition with no effective treatments.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.