Provider Name
Service provider

Al Hayat Medical Laboratories - Jeddah

Showing 421 to 441 of 652 entries
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Tests

TORCH IgM Profile

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Huntington Genetic Testing

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Cockayne Syndrome

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L-2-Hydroxyglutaric Aciduria (L2HG DH gene Sequenc

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Cornelia de Lange Syndrome gene Panel by NGS

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Congenital ichthyosis gene Panel (9 genes): includ

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Congenital Ichthyosis ABCA12 gene sequencing

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Dystonia gene Panel Next generation gene sequencin

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Ichthyosis, lamellar type 1 gene TGM1 full gene se

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Primary Dystonia Evaluation: TOR1A (DYT1) gene and

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Prenatal diagnosis of a single gene disorder with

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Achondroplasia (FGFR3) Sequencing

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Alstrom syndrome (ALMS1) Sequencing

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Arginase deficiency (ARG1) Sequencing

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Von wille brand Factor activity (Ristocetin Cofactor)

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Glutamate Decarboxylase Abs in serum (Anti GAD)

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Tacrolimus (FK506)

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Erythropoietin (EPO)

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CA 50

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Dopamine Beta Hydroxylase

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N-methyl-D-Aspatate Receptor (IgG)

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