{"id":20540,"date":"2024-01-24T15:16:28","date_gmt":"2024-01-24T14:16:28","guid":{"rendered":"https:\/\/www.fennerlabor.de\/klinische-chemie\/beta-galaktosidase\/"},"modified":"2024-01-24T15:16:29","modified_gmt":"2024-01-24T14:16:29","slug":"beta-galaktosidase","status":"publish","type":"lab_clinical_che","link":"https:\/\/www.fennerlabor.de\/klinische-chemie\/beta-galaktosidase\/","title":{"rendered":"Beta-Galaktosidase"},"template":"","meta":{"_acf_changed":false},"acf":{"synonyms":"\u03b2-Galactosidase","parameter":"","sample_material":"ca. 1,0 ml Serum\nca. 1,0 ml Liquor","tube":"","preanalytics":"Das Blut bitte innerhalb von 30 Minuten nach der Abnahme zentrifugieren, Serum in ein separates R\u00f6hrchen abpipettieren und einfrieren (ca. - 20\u00b0C), Liquor direkt nach der Abnahme einfrieren.","implementation_notes":"","sample_transport":"Botendienst erforderlich, Probentransport tiefgefroren (ca. - 20\u00b0C)","references":"","clinical_indications":"Sphingolipidspeicherkrankheit","method":"Fremdleistung","approach_days":"","reference_ranges":"","source_reference_ranges":"","notes":"\u03b2-Galaktosidase-Mangel: generalisierte Gangliosidose (autosomal-rezessiv vererbt), Lipidspeicherkrankheit aus der Gruppe der Sphingolipidosen mit geistiger Retardierung und weiteren Organmanifestationen","cross_references":"Alpha-Galaktosidase","comments":"","additional_claims":"","increased_values":"","decreased_values":"","loinc_number":"","accounting_ebm":"","billing_goa":"","accreditation":"Ja","fennerlabor_department":"","internal_laboratory_edp_id":"","external_laboratories":"Labor Wittke\/Gerritzen","internal_remarks":""},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.4 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Beta-Galaktosidase - Labor Dr. Fenner &amp; 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