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A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

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.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Inhibiting 5α-reductase during late pregnancy shortens gestation, reduces litter size, and harms memory in rat offspring.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

A specific gene mutation causes sparse, brittle hair in a family.

DHEA treatment helps grow pubic hair and boosts mood in girls with adrenal issues.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Hypothyroidism patients with hair loss typically have thinning hair, smaller hair follicles, and normal hair shedding.

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

Malnutrition severely harms growth and development in young baboons.

Severe hypothyroidism can cause temporary liver and kidney issues, which improve with thyroxine treatment.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

A deer fawn in South Dakota was the first cervid found with congenital hypotrichosis, a condition causing sparse or missing hair.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

The woman's symptoms were due to an androgen-secreting tumor, not PCOS.

A chubby child can still be malnourished.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

Genetic testing for EGFR mutations is crucial in similar cases.

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

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

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

DHEA therapy improves pubic hair growth and psychological well-being in young females with central adrenal insufficiency.

A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.