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BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

Men with certain types of baldness at age 45 may have a higher risk of colon cancer and colorectal adenoma.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

HIV can cause skin disorders, which are often the first sign of infection, especially in people with darker skin.

No genetic link between prostaglandins and hair loss found.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

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

Inflammatory skin conditions are the most common in Brazilian children, with atopic dermatitis being the top issue.

Acitretin helped improve hand mobility and skin condition in a patient.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

A 3-year-old girl developed scurvy symptoms that improved with vitamin C but relapsed when supplementation stopped.

Healthcare providers should start with simple fertility tests and treatments before referring patients to specialists.

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

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

CD2 might be a new treatment target for patchy alopecia areata.

FUE megasession effectively treats severe hair loss with natural-looking results in one operation.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

Twins had rare skin cysts likely due to genetics.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.