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

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

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

Most inconsolable crying in infants is not due to a serious cause, and a detailed check-up is typically enough to find the reason.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Hair loss can be an early sign of Crohn's disease in children.

Chlormadinone acetate is a strong, well-tolerated hormone used in birth control and hormone therapy with benefits for menstrual pain and skin conditions.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

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

Gynecomastia and premature thelarche often resolve naturally but need evaluation to rule out serious issues.

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.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

Genetic testing for EGFR mutations is crucial in similar cases.

A 5-year-old girl's scalp scarring and hair loss from lupus improved with specific medications.

Obesity and certain hormone levels can lead to advanced bone age in young girls with early breast development.

A girl had rickets due to a gene mutation affecting vitamin D response.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

A toddler who accidentally swallowed hair growth medicine experienced serious heart-related side effects but recovered after hospital treatment.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Many children and teens referred to gender services receive hormone treatments, but more research is needed on their long-term care and outcomes.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A 9-year-old boy had a calcium deposit nodule on his earlobe.

Children need early diagnosis and treatment for iron-deficiency anemia to prevent learning problems and promote health.