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1 records shown · first 60Sphingolipid activator protein B deficiency: report of 9 Saudi patients and review of the literature.
PMID 19955343 | DOI 10.1177/0883073809341269 · Journal of child neurology · 2009 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | C241S | “PSAP analysis found that the 4 families segregate the same homozygous mutation that was a g.722G>C transversion resulting in C241S change, which was previously reported in an Arab patient.” | 0.82 | literature_variant_regex_v2 |
| gene | PSAP | “Mutated PSAP gene resulting in sphingolipid activator protein B deficiency is known to cause metachromatic leukodystrophy variant in which arylsulfatase A is normal.” | 0.98 | hgnc_dict_v1 |
| population | Saudi Arabia | “Sphingolipid activator protein B deficiency: report of 9 Saudi patients and review of the literature. Of 16 patients with metachromatic leukodystrophy that were evaluated in our center, 7 patients were diagnosed with arylsulfatase A-deficient metachromatic leukodystrophy, whereas 9 children from 4 unrelated Saudi families were found to have sphingolipid activator protein B deficiency.” | 0.95 | saudi_context_rules_v1 |
| variant | g.722G>C | “PSAP analysis found that the 4 families segregate the same homozygous mutation that was a g.722G>C transversion resulting in C241S change, which was previously reported in an Arab patient.” | 0.95 | hgvs_regex_v1 |