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Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Ritlecitinib helped most alopecia areata patients regrow hair by Week 48.

BMI1 is essential for preventing hair greying and maintaining hair color.

Human hair follicles can assess carcinogen metabolism and imidazole compounds might be effective anticarcinogens.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

Androgen suppression therapy (AST) doesn't significantly lower bladder cancer risk, but using finasteride, a type of AST, might decrease the risk. AST also lessens the chance of cancer coming back but doesn't really affect survival rates. More research is needed to understand AST's benefits for different bladder cancers.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

M1 homeopathic complex may help slow melanoma cell growth.

Ritlecitinib was generally well tolerated in children with alopecia areata.

Zinc chloride can cause human scalp cells to multiply and die.

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

Immunomodulatory therapies are effective for treating cutaneous lymphoma, particularly in early stages.

Three genes linked to the development of trichilemmal cysts were found.

Taking Vitamin D with clomiphene citrate significantly improves ovulation in women with Poly Cystic Ovary Syndrome.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

A man's skin cancer improved and some of his hair grew back after treatment with a special light therapy and a medication.

Clonally expanded CD8+ T cells cause alopecia areata.

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

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

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

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.