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1999, Number 4

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Rev Mex Pediatr 1999; 66 (4)

Lisencefalia tipo I: síndrome de Miller-Dieker. Informe de un caso

López HJF, García RR, Pérez ZMÁ

Language: Spanish
References: 12
Page: 157-160
PDF size: 631.18 Kb.


ABSTRACT

We report of an infant with a pregnant mother’s background of two abortion menaces; that shows a generalized hypotonia with abnormal facies, lower ear positioning, micrognathia, no visual following, auditive lack, ape pleat, decreasing miotatic reflexes. Electroencephalography (EEG), cranial computed tomography (TAC), craneal magnetic resonance (RM), single-photon emission computed tomography (SPECT) and evoked auditory and visual potentials were realized.
It includes neuronal migration disorders (NMD) of type lissencephaly and associated to dismorphic stigmas, Miller-Dieker syndrome was set up.


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