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Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Mutations in the KRT85 gene cause hair and nail problems.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Haplogroup X found in Altaian population supports Amerindian origin.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Mutation in hairless gene may increase hair loss risk.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Mutation in hairless gene may increase hair loss risk.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Furless male rabbits grew slightly faster and heavier than furred ones, but testosterone levels were not the cause.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

A boy with a rare skin condition improved quickly after starting zinc supplements.

Leontopodium alpinum extract may help reduce hair shedding by keeping hair in the growth phase longer.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.