RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164084838
T1 Seitelberger Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164084838
RD 2024/04/20
AB A  very  rare  degenerative  encephalopathy  with  associated  visceral  malformations.  Demyelinating  disease  with  early  onset  and  absence  of  stainable  myelin.  The  affected  child  is  normal  at  birth  and  development  is  normal  until  2  years  of  age.  Motor  dysfunction  manifests  by  difficulty  standing  and  walking,  progressive  deterioration  of  neurological  function  and  speech,  nystagmus,  strabismus,  optical  atrophy,  seizures,  and  areflexia.