RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164073436
T1 Hypomelanosis of Ito
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=1164073436
RD 2024/04/19
AB Congenital  disorder  characterized  by  hypopigmented  whorls  of  skin  along  the  line  of  Blaschko  and  associated  with  multiple  other  congenital  defects,  mostly  neurologic,  skeletal,  ophthalmic,  hair,  and  dental  anomalies.  Seizures,  severe  developmental  delays,  and  musculoskeletal  symptoms  (scoliosis)  are  commonly  associated  with  this  condition.