| LastName | Melegh |
| FirstName | Bela |
| Bela.Melegh@aok.pte.hu | |
| OrganizationName | Dept. of Medical Genetics and Child Development |
| Country | Hungary |
| Address | University of PecsĂșculty of Medicine%Szigeti u. 12.%H-7624 Pecs |
| PILastName | Melegh |
| PIFirstName | Bela |
| PIEmail | Bela.Melegh@aok.pte.hu |
| OtherContributor | Bene, Judit; Komlosi, Katalin; Havasi, Viktoria |
| PolymorphismPosition | 15310 |
| Polymorphism | C |
| AlleleType | polymorphism |
| NAChange | T-C |
| AAChange | syn |
| Locus | MT-CYB |
| Detection | automated |
| SampleID | BI 7.8.1.0.0.6/2 |
| Tissue | blood |
| Phenotype | Myopathy (unknown), Bilateral Ptosis |
| Ethnicity | Caucasian |
| Origin | Hungary |
| Haplogroup | - |
| Comment | Our patient presented with the following symptoms: muscle weakness,bilateral ptosis, short stature, facial anomalies, mental retardation,radiologic evidence of pitutary hypoplasia. No definitive diagnosis was established so far. The following polymorphisms were detected in the mitochondrial genome:14470 T-C, 15310 T-C, none of which cause an amino acid change. |
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