TYROSINEMIA, TRANSIENT, OF THE NEWBORN

Question 1

What is  TYROSINEMIA, TRANSIENT, OF THE NEWBORN?

Accepted Answer

benign benign disorder of tyrosine metabolism, detected upon newborn screening, often observed in premature infants, no clinical symptoms

Question 2

Gibt es eine deutsche Bezeichnung?

Accepted Answer

Transiente Tyrosinämie beim Neugeborenen

Question 3

What is the link to OMIM ?

Accepted Answer

OMIN ---

Question 4

Which enzymes are involved?

Accepted Answer

delayed enzyme maturation

Disease	TYROSINEMIA, TRANSIENT, OF THE NEWBORN
Synonym	TYROSINE METABOLISM, DELAYED MATURATION IN
OMIM	--- OMIM = Online Mendelian Inheritance of Men
Orphanet	3402
Gene locus	--- Detail information to gene locus by the National Center for Biotechnology Information NCBI: MAJOR HISTOCOMPATIBILITY COMPLEX
ICD	P74.5
Summary	benign benign disorder of tyrosine metabolism, detected upon newborn screening, often observed in premature infants, no clinical symptoms
Laboratory findings	4-Hydroxyphenylpyruvic acid inc (urine) L-Tyrosine inc (plasma) 4-Hydroxyphenylacetic acid inc (urine) 4-Hydroxyphenyllactic acid inc (urine)
Symptoms	Amino acids, plasma no clinical symptoms (probably) onset, neonatal Organic acids, urine