RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164076147
T1 Laband 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=1164076147
RD 2024/04/24
AB Inherited  polymalformative  syndrome  characterized  by  craniofacial  anomalies  with  gingival  fibromatosis  and  dystrophic  fingers  and  fingernails.  The  clinical  characteristics  are  gingival  fibromatosis  that  is  present  at  birth  or  in  the  days  following  it,  severe  hypoplasia  of  the  distal  phalanges  of  the  hands  and  feet,  dysplasia  of  the  nail,  joint  hypermobility,  and  hepatosplenomegaly.  Other  features  include  a  nose  and  pinnae  usually  large  and  poorly  developed.  It  is  often  associated  with  mental  retardation.