Author/Authors :
Sertac Arslanoglu، نويسنده , , Mehmet Yalaz، نويسنده , , Damla G?k en، نويسنده , , Mahmut Coker، نويسنده , , Sarenur Tütüncüo lu، نويسنده , , Mete Ak?su، نويسنده , , ükran Darcan، نويسنده , , Nilgun Kultursay، نويسنده , , Metin Ciri ، نويسنده , , Eren Demirta ، نويسنده ,
Abstract :
Molybdenum cofactor deficiency is a rare and devastating disease leading to intractable seizures in the neonatal period. Severe loss of neocortical neurons, gliosis, and cystic necrosis of cerebral white matter resulting in significant cerebral volume loss are the neuropathological findings. The mechanism of cerebral injury is unknown, but sulphite excess, and sulphate or uric acid deficiencies are possible factors. We present here a new case of Molybdenum cofactor deficiency associated with Dandy–Walker complex with a history of three dead siblings, the latter also having Dandy–Walker malformation. We speculate that severe cerebral volume loss due to the above mentioned mechanisms may lead to an appearance resembling Dandy–Walker malformation.
Keywords :
Dandy–Walker malformation , Neonatal seizures , Dandy–Walker complex , Molybdenum cofactor deficiency