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Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Right hand finger ratio may predict male hair loss.

Finger length ratio may indicate male hair loss.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Neurotrophins, especially NGF, are crucial for pain development and management.

Mouse genital development depends on male or female hormones for specific features.

Higher early lead exposure is linked to delayed puberty in girls.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Microglia, the brain's immune cells, may contribute to Polycystic Ovary Syndrome (PCOS) by altering the female brain's structure and function, with kisspeptin neurons and GABA neurotransmitters also playing a role.

A baby girl had two brain-related growths removed and is developing normally.

Early over-expression of FoxN1 harms immune and skin development.

High levels of androgens during early development may cause PCOS-like symptoms.

Recent progress has been made in understanding inherited hair and nail disorders.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

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

Doctors are preparing to potentially perform uterus transplants in transgender women, considering technical, hormonal, and ethical factors.

Fetal skin has unique immune cells different from adult skin.

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

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Inclusive and affirming healthcare is essential for improving transgender individuals' quality of life and health.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Certain finger length ratios and body hair patterns may predict side effects from birth control pills in women.

The conclusion is that hair supplement ingredients may be unsafe and should be disclosed and proven safe before use.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

Older age, higher BMI, and family history of diabetes increase the risk of gestational diabetes in pregnant women.

Hedgehog signaling is crucial for mammary gland development over hair follicles.