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After chemotherapy for a gestational trophoblastic tumor, normal pregnancy rates are possible, but there's a slightly higher risk of the tumor reoccurring in future pregnancies.

Postmenopausal ovary stromal cells have a unique makeup and limited steroid production, suggesting androgens come from the adrenal gland.

Diagnosing and treating skin conditions is challenging, especially when drug reactions mimic other diseases.

Finasteride, a drug used for certain conditions, can cause serious side effects like sexual dysfunction, suicidal thoughts, and increased diabetes risk, and there's a need for more awareness and research about these effects.

Oral contraceptives often cause melasma and other skin issues.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A child used a hair growth lotion for hair loss, but it caused excessive hair growth on his face and neck instead.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

FGF13 gene changes cause excessive hair growth in a rare condition.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Tofacitinib helped regrow hair in a patient with severe hair loss and improved their quality of life without side effects.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

PRP injections are not effective for long-term treatment of temporal triangular alopecia.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Improper use of ceramic flat irons can cause severe hair damage.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

OCT is a reliable, noninvasive way to measure hair thickness.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Hair splitting and nail detachment are linked conditions.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Some drugs can cause changes to your hair.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Telogen effluvium is a condition that causes temporary hair loss.