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Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Dupilumab significantly improved a 5-year-old girl's prurigo nodularis without side effects.

Congenital atrichia with papular lesions causes permanent hair loss in children.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

The AAcQLI is a promising tool for assessing quality of life in children with alopecia areata.

A rare skin condition in children can look like other diseases.

Careful diagnosis is crucial for premature pubarche, as 20% of cases have other conditions.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

The boy's symptoms suggest a possible new medical condition.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Recombinant gonadotropins improve future fertility in CHH patients.

Identifying and treating deficiencies and conditions can stop or reverse premature greying in children.

Identifying and treating deficiencies and conditions can stop or reverse premature greying in children.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Red light therapy temporarily increased blood flow in the eye but didn't change other eye structures.

A 4-year-old girl's hair loss stopped after taking zinc supplements and changing her diet.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Hair restoration in children, tailored to their specific needs, can yield good aesthetic results with minimal complications.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Zinc effectively treats most children with acrodermatitis enteropathica, but underlying metabolic issues may require additional management.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Recurrent dry cough, wheezing, and respiratory discomfort are key symptoms for diagnosing pediatric asthma.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Topical diphencyprone effectively treated a 9-year-old boy's alopecia areata with fewer side effects.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

The study concludes that as skin matures from infancy to childhood, there are major changes in cell differentiation, stemness, and growth, leading to a stronger skin barrier in older children.