TY  - CHAP
M1  - Book, Section
TI  - Chapter 136. Disorders of Tyrosine Metabolism
A1  - Schwahn, Bernd Christian
A2  - Rudolph, Colin D.
A2  - Rudolph, Abraham M.
A2  - Lister, George E.
A2  - First, Lewis R.
A2  - Gershon, Anne A.
Y1  - 2011
N1  - 
T2  - Rudolph's Pediatrics, 22e
AB  - The  five  known  inherited  disorders  in  the  metabolism  of  the  nonessential  amino  acid  tyrosine  are  each  very  rare  and  present  in  different  ways.  Four  of  them  share  a  degree  of  hypertyrosinemia,  but  this  sign  is  not  specific  and  can  also  be  found  in  other  conditions  such  as  transient  tyrosinemia  of  the  preterm  newborn,  which  results  from  delayed  maturation  of  tyrosine-metabolizing  enzymes;  in  scurvy;  and  in  many  forms  of  general  liver  disease.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=6724599
ER  -