Search

everythinglearnresearchcommunity

for

Search:↓

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

A new genetic mutation was found causing hair and eye issues in a boy.

The infant's hair loss resolved naturally by 20 months without treatment.

Delayed puberty often runs in families, can affect growth, and may need hormone treatment.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Children with alopecia areata should only get thyroid screening if they have Down syndrome, a family history of thyroid disease, atopy, or signs of thyroid problems.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A rare form of alopecia causes hair thinning without bald spots and may be more common than thought, responding well to steroid treatment.

Some teenagers with anorexia nervosa have worse cognitive abilities, especially in visual and spatial tasks, and this is more common in those with a lower body weight.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

Finasteride's sexual side effects not caused by androgen deficiency or SRD5A inhibition.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Alopecia areata severity in children is linked to atopy history, disease duration, and nail involvement, but not anemia.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.

Hypothyroidism slows metabolism, causing growth and mental issues in children and reversible symptoms in adults, needing early treatment.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Early and proper treatment is crucial for children with allergic conjunctivitis to avoid complications.

The boy's hair and skin color differences are due to a pigmentation disorder.

Alopecia areata has different forms and can significantly affect quality of life, especially in more severe cases.

An 11-month-old girl has no scalp or body hair, and the cause is being studied.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

Diagnosing PCOS in teenagers is challenging and should use strict criteria to avoid misdiagnosis and unnecessary worry.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Spironolactone is effective for treating acne, hirsutism, and androgenic alopecia in women with few side effects.