-
Hyperlysinemia is an
autosomal recessive metabolic disorder characterized by an
abnormal increase of
lysine in the blood, but
appears to be benign. It...
-
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...
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syndrome Sulfite oxidase deficiency Molybdenum cofactor deficiency Hyperlysinemia Less common: Ehlers–Danlos
syndrome Crouzon disease Refsum syndrome...
- 2017-03-05.
Markovitz PJ,
Chuang DT, Cox RP (October 1984). "Familial
hyperlysinemias.
Purification and
characterization of the
bifunctional aminoadipic...
-
Hyperlipoproteinemia type IV
Hyperlipoproteinemia type V
Hyperlipoproteinemia Hyperlysinemia Hyperopia Hyperornithinemia Hyperornithinemia, hyperammonemia, homocitrullinuria...
-
Hyperammonemia 270.7
Disorders of straight-chain amino-acid
metabolism Hyperlysinemia Pipecolic acidemia Saccharopinuria 270.8
Other specified disorders of...
- 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...
