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Most patients with chronic kidney disease have skin problems, which get worse as the disease progresses, and dialysis doesn't greatly reduce these issues.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Ultrasound is a useful, non-invasive tool in dermatology for diagnosing skin conditions and guiding treatments, but it has some limitations.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

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

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Light microscopy is useful for diagnosing different hair disorders.

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

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

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

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Dermoscopy has improved skin cancer diagnosis and has expanding applications in dermatology, but requires staying updated with new research and techniques.

Dermoscopy has greatly improved the diagnosis of skin lesions and our understanding of their morphology and biology.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Pregnancy can cause various skin changes, including pigmentation, acne, and stretch marks, and may affect preexisting skin conditions.

The document discusses how to identify and manage common skin conditions in children.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Most patients with chronic kidney disease had skin issues like paleness and dry skin, and treating these can improve their lives.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Six genetic conditions are often linked to complete scalp hair loss in children.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.