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Meckel syndrome
Meckel syndrome is a rare, lethal, ciliopathic, genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations, polydactyly, hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios.
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Ciliopathy
Congenital disorders of urinary system
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Nephrology
Hepatology
Autosomal recessive disorders
Rare diseases
Neurological disorders
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