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. |