[…] are stillborn or die in early neonatal period, 14% survive GREIG CEPHALOPOLYSYNDACTYLY (GCPS) Responsible gene: GLI3 Protein: Zinc finger protein GLI3 Cytogenetic locus:
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7p13 Inheritance: AD Clinical Features and Diagnostic Criteria: Major findings: macrocephaly, ocular hypertelorism, preaxial polydactyly, cutaneous syndactyly.
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[…] hypoplasia, ID in survivors, agenesis of the CC, optic and olfactory tract hypoplasia, encephalocele, GU malformation Disease Mechanism: unknown Treatment/Prognosis: The majority
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