Hinman syndrome is a rare congenital disorder characterized by the presence of multiple malformations, including cleft lip and palate, extra fingers and toes, and kidney and urinary tract abnormalities. It is caused by a mutation in the HOXA13 gene.

The primary symptom of Hinman syndrome is a severe, Burning Pain in the lower abdomen and groin area. Other symptoms may include:

-Frequent urination
-Painful urination
-Blood in the urine
-Fever
-Nausea
-Vomiting
-Abdominal swelling
-Abdominal tenderness
-Painful intercourse
-Painful bowel movements
-Constipation
-Diarrhea
-Fatigue
-Weight loss

Hinman syndrome is a rare congenital disorder caused by a mutation in the HOXA13 gene. This gene is responsible for the development of the urinary tract and reproductive organs. The exact cause of the mutation is unknown, but it is believed to be due to a combination of genetic and environmental factors.

The primary treatment for Hinman syndrome is physical therapy. Physical therapy can help to improve range of motion, strength, and coordination. Other treatments may include medications to reduce inflammation, injections of corticosteroids to reduce inflammation, and surgery to correct any underlying structural issues. In some cases, bracing may be recommended to help support the affected joint.

1. Previous history of urinary tract infection
2. Male gender
3. Young age
4. Immunosuppression
5. Diabetes
6. Structural abnormalities of the urinary tract
7. Use of catheters
8. Use of antibiotics
9. Use of immunosuppressive drugs
10. Use of corticosteroids

At this time, there is no known cure for Hinman Syndrome. Treatment typically involves physical therapy, occupational therapy, and speech therapy to help manage the symptoms. Medications may also be prescribed to help reduce muscle spasms and pain.