A 3-month-old female was referred for evaluation of bilateral eyelid abnormalities. There was a strong family history of congenital eyelid abnormalities including her father, paternal aunt, and paternal grandfather.
1. What is the diagnosis and what are the characteristic findings?
2. What are the associated findings in this condition?
3. Describe the genetics and pathogenesis of the condition?
4. What is the differential diagnosis?
5. What is the treatment?