RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164079143
T1 Monilethrix
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=1164079143
RD 2024/04/24
AB It  is  a  genetic  disorder  affecting  the  hair  and  occasionally  the  skin.  Patches  of  alopecia  may  be  present.  It  does  not  belong  to  the  group  of  ectodermal  dysplasias.  The  onset  of  the  disease  is  at  birth  or  within  the  first  2  years  of  life.  In  some  cases,  the  symptoms  may  improve  at  puberty  or  during  pregnancy;  in  other  cases,  the  symptoms  may  remain  the  same  throughout  life.