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Fig. 6 | Orphanet Journal of Rare Diseases

Fig. 6

From: Further evidence for POMK as candidate gene for WWS with meningoencephalocele

Fig. 6

Postnatal cranial MRI scan (performed at 2nd / 3rd day); clinical findings: occipital meningocele with dorsal enlarged 4th ventricle (white arrow picture a), vermis hypo−/aplasia (white arrow picture b), generalized polymicrogyria-like cobblestone malformation, temporo-occipital subcortical band heterotopia, eye malformations (G1: microphthalmia with coloboma and caudal cyst, G2: persistent hypoplastic primary vitreous body and posterior staphyloma). a/c = G1, b/d = G2

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