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Exposure to the hair loss drug finasteride during pregnancy can cause genital anomalies in male babies, but not in female babies. It's best to avoid this drug in women who could potentially become pregnant.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Adult offspring of sperm donation generally feel positive about their conception and view the donor as their biological father.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Hair transplantation is safe and effective for children with scar-related hair loss.

Alopecia Areata greatly affects the quality of life and mental health of Canadian patients and their caregivers.

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

Sodium valproate effectively reduces seizures in children with epilepsy, especially in primary generalized cases.

Children's hair care needs gentle products and better regulations due to unique hair and scalp differences.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Trichotillomania in children is a sign of emotional distress needing tailored treatment and family support.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

A young girl's foot lesion was actually a rare condition caused by a hair fragment under the skin, not a parasite.

Neutrophils quickly respond to skin injury.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Neutrophils quickly move to the site of skin injury.

An 11-year-old girl with Kawasaki disease experienced hair loss that improved after treatment.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

A woman with PCOS successfully overcame secondary infertility and became pregnant with triplets after treatment.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A toddler with unusual hypothyroidism symptoms improved with levothyroxine treatment.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

People with Down's syndrome are more likely to have syringomas.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

A 9-month-old baby had a rare, persistent ring-shaped hair loss condition.

Parents often know about skin care, but children with less educated, lower-income parents have more skin problems.

Older age, obesity, hirsutism, and having children increase metabolic risk in women with PCOS.