RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164060282
T1 Acrocephalopolysyndactyly Type IV: Goodman 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=1164060282
RD 2024/04/19
AB Extremely  rare  genetic  disorder  characterized  by  marked  malformations  of  the  head  and  face,  polysyndactyly,  and  congenital  heart  defects,  which  may  result  in  early  death.  This  syndrome  includes  ulnar  deviation  of  digits  II  and  III  and  clinodactyly  and  camptodactyly.  Goodman  Syndrome  is  now  considered  to  be  a  variant  of  Carpenter  Syndrome.