RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164068735
T1 Ectrodactyly, Ectodermal Dysplasia, and Clefting (EEC) Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164068735
RD 2024/04/19
AB Autosomal  dominant  inherited  syndrome  characterized  by  the  triad  of  ectrodactyly,  ectodermal  dysplasia,  and  facial  clefts  (lip  and  palate).  Other  clinical  features  include  maxillary  hypoplasia,  mild  malar  hypoplasia,  choanal  atresia,  conductive  hearing  loss,  photophobia  and  blepharophimosis,  dacryocystitis,  cryptorchidism,  hypogonadotropic  hypogonadism  renal  agenesis  or  dysplasia,  hydronephrosis,  occasionally  mental  retardation,  central  diabetes  insipidus.