RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164081997
T1 Pollitt 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=1164081997
RD 2024/04/18
AB Inherited  syndrome  characterized  by  trichorrhexis  nodosa,  psychomotor  retardation,  microcephaly,  and  the  deficiency  of  high-sulfur  protein  in  the  hair.