RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164083727
T1 Riley-Smith 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=1164083727
RD 2024/04/20
AB A  rare  malformation  syndrome  characterized  by  Macrocephaly,  Autosomal  dominant,  Thyroid  disease,  Cancer,  Hamartomata,  Skin  abnormalities  (MATCHS)  and  due  to  mutations  of  the  PTEN  tumor  suppressor  gene  (an  acronym  that  stands  for  Phosphatase  and  TENsin  homolog  deleted  on  chromosome  TEN).  Multiple  hemangiomata  and  lipomas.  Subcutaneous  hemangioma  may  be  present  at  birth  or  appear  later  in  childhood.