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Figure 5 | Orphanet Journal of Rare Diseases

Figure 5

From: Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech gypsy children – frequent and underestimated cause of disability among Czech gypsies

Figure 5

Patient 4 at the age of 3.5 years. The patient is a sporadic case in the family. He has no siblings. Prenatal screening revealed megaurether and hydronephrosis in this patient. Congenital cataract was surgically corrected at the age of three months. He was able to sit at 13 months of age and walk at 2.5 years. He is able to use simple sentences.

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