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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

The shape and size of the placenta may help predict future health risks for both mother and child.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Fetuin A may increase collagen production and promote scarring.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Early diagnosis of imperforate hymen is crucial to prevent complications.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Maternal hypothyroidism harms skin development in rat offspring.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

Finasteride-treated male rats' offspring had altered glucose metabolism, potentially increasing diabetes risk.

Iron-deficiency anemia in pregnancy can cause serious health issues for both mother and baby.

Nail abnormalities in children can indicate deeper health issues.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Father's finasteride use may affect son's fertility and testicular function.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Methimazole may cause skin defects in babies if taken during pregnancy.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A rare benign scalp tumor in an infant requires surgical removal.