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A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

PCFCL may have unrecognized subtypes and needs more research.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Children with atopic dermatitis often have sleep problems due to itching and may benefit from melatonin, which helps with sleep and skin symptoms.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

A vitamin D receptor mutation causes rickets and affects immune responses.

A hairless patch on a boy's scalp from birth injury improved with minoxidil treatment.

Zinc deficiency in children can cause skin issues and is often overlooked.

New treatments for skin conditions in children include a preferred drug for birthmark reduction, proactive creams for eczema and vitiligo, a safe psoriasis medication, and special tissues and socks for eczema and fungal infections.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Most pediatric cancer patients at Muhimbili National Hospital experienced adverse drug reactions during chemotherapy, highlighting the need for careful monitoring.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Cross-sex hormone therapy is important for managing gender dysphoria and requires careful monitoring and healthcare provider education.

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

The Edwardian medical campaign linked maternal drinking to infant mortality and national decline, influencing hygiene education and leading to a ban on children under 14 from pubs.

A 24-month-old Nigerian girl developed early puberty with no family history, needing treatment her family couldn't afford.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Early exposure to fluoride, lead, and certain nutrients affects puberty differently in boys and girls.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Medical care for transgender youth should be individualized and supportive.

More pediatric-specific research and guidelines are needed to improve hidradenitis suppurativa treatment in children and adolescents.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The young goat had anaplasmosis and copper deficiency.

Skin symptoms are important for diagnosing and managing juvenile-onset systemic lupus erythematosus and usually get better with treatment.

Allergic skin issues are most common in children, and understanding these problems should be prioritized.

Zinc supplements can help skin issues even if blood zinc levels are normal.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

The boy's scurvy symptoms improved with vitamin C treatment, highlighting the need for a balanced diet.