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

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

The letter agrees that adults can get contact alopecia, which improves with allergen avoidance, and stresses early diagnosis to prevent permanent hair loss.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Two children with lysinuric protein intolerance showed symptoms similar to lupus.

Alopecia areata in infants may be more common than previously thought.

The book "Baby Skin" provides useful skin care guidance for parents and is well-received despite lacking visual aids.

Certain maturity signs appear before and after the first release of sperm in boys.

Hair bands are a new symptom of facio-genito-popliteal syndrome.

The document concludes that some dermatology books are useful for their photos or specific topics, while others have limitations like poor quality images or content.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Patients with anorexia nervosa did not show a correlation between zinc levels and taste perception or the severity of their condition.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

A baby girl had two brain-related growths removed and is developing normally.

A 1-year-old boy developed excessive hair growth from exposure to a hair growth treatment.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

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

An infant with scalp fungus was cured after extended treatment with antifungal medication.

COVID-19 can cause skin problems in children.

A girl with Crohn's disease developed hair loss from her medication, which improved with treatment but later returned.

Hair loss may be a delayed side effect of Multisystem Inflammatory Syndrome in children after COVID-19.

Most children recovered from COVID-19 in 4 weeks, but some experienced long-term symptoms, especially older kids.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.