-
Hyperlysinemia is an
autosomal recessive metabolic disorder characterized by an
abnormal increase of
lysine in the blood, but
appears to be benign. It...
- 2017-03-05.
Markovitz PJ,
Chuang DT, Cox RP (October 1984). "Familial
hyperlysinemias.
Purification and
characterization of the
bifunctional aminoadipic...
-
Citrullinemia Hyperargininemia Hyperhomocysteinemia Hypermethioninemia Hyperlysinemias Nonketotic hyperglycinemia Propionic acidemia Hyperprolinemia Cystinuria...
- spasticity, and
psychomotor impairment. The
clinical significance of
hyperlysinemia is the
subject of
debate in the
field with some
studies finding no correlation...
- IDUA 1:100,000 Hutchinson–Gilford
progeria syndrome LMNA 1:18,000,000
Hyperlysinemia A****
recessive Hyperoxaluria,
primary AGXT, GRHPR,
DHDPSL Hyperphenylalaninemia...
-
hypusine was
found in the
urine of
children and
patients with
familial hyperlysinemia.
Hypusine was
first isolated from
bovine brain by ****anese scientists...
- reductase.
Lysine degradation is also
affected in this
disorder leading to
hyperlysinemia. The
disorder is
inherited in an
autosomal recessive manner, meaning...
-
syndrome Sulfite oxidase deficiency Molybdenum cofactor deficiency Hyperlysinemia Less common: Ehlers–Danlos
syndrome Crouzon disease Refsum syndrome...
- PMID 4385118.
Markovitz PJ,
Chuang DT, Cox RP (1984). "Familial
hyperlysinemias.
Purification and
characterization of the
bifunctional aminoadipic...
- PMID 4385118.
Markovitz PJ,
Chuang DT, Cox RP (1984). "Familial
hyperlysinemias.
Purification and
characterization of the
bifunctional aminoadipic...
