2008年度國內各醫院送檢結果統計表 |
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編號 |
醫院 |
疑似疾病診斷 |
檢驗機構/項目/國家 |
檢驗結果/日期 |
|
1 |
台中榮總 |
AADC |
Horizon Molecular Medicine/ AADC enzyme assay/美國 |
|
|
2 |
台中榮總 |
AADC |
Horizon Molecular Medicine/ AADC CSF
neurotransmitter/美國 |
|
|
3 |
馬偕醫院 |
OTC |
Children's National Medical Center/ Allopurinol test /美國 |
Carrier/ 96.12.28 |
|
4 |
台大醫院 |
FSHD |
Athena Diagnostics/ FSHD DNA test/美國 |
FSHD/ 96.12.27 |
|
5 |
台大醫院 |
HSP |
Athena Diagnostics/ SPG4, SPG |
HSP(SPG4) mutation/ 96.12.30 |
|
6 |
台大醫院 |
FSHD |
Athena Diagnostics/ FSHD DNA test/美國 |
No mutation/ 96.12.27 |
|
7 |
台大醫院 |
CF |
Canterbury Health Laboratories/ CF 29 arms assay & DHPLC/紐西蘭 |
CF patient(homozygous for c.1766+ |
|
8 |
台大醫院 |
CF |
Canterbury Health Laboratories/ CF 29 arms assay & DHPLC/紐西蘭 |
Carries one copy of each of the polymorphisms
C.1210-34TG,this result dose not support a
diagnosis of CF/97.02.01 |
|
9 |
台大醫院 |
Mitochondrial disorders |
Baylor College of Medicine/ SCO1 sequencing/美國 |
No mutation/ 97.01.30 |
|
10 |
台大醫院 |
Alstrom syndrome |
Centogene GmbH/ ALMS1 gene sequencing/ 德國 |
ALMS gene 19bp deletion/ 97.04.25 |
|
11 |
高雄長庚 |
Organic Acidemias |
Lab Genetic Metabolic Disease. Academic Medical Center
University/ 3-Methylglutaconyl-CoA Hydratase enzyme assay/荷蘭 |
|
|
12 |
台中榮總 |
Congenital generalized lipodystrophy |
Institut de Pathologle et de Genetlque
Centre/ BSCL1 genes mutation analysis/ 比利時 |
Bscl2 gene no mutation and Bscl1 gene is in progress |
|
13 |
中國醫藥大學 附設醫院 |
Wilson's disease |
Mayo medical laboratories/ ATP7B DNA seuencing/美國 |
T |
|
14 |
台中榮總 |
Carnitine deficiency syndrome |
Mayo Medical Lab./ Fatty acid probe assay/美國 |
Normal/96.08.13 |
|
15 |
台中榮總 |
Carnitine deficiency syndrome |
Mayo Medical Lab/ Fatty acid probe assay/美國 |
|
|
16 |
花蓮慈濟醫院 |
MSUD |
Woman's & Children's Hospital / branched-chain
amino acids enzyme assay/澳州 |
Fetus is not affected by MSUD / 96.11.15 |
|
17 |
台大醫院 |
Cockayne syndrome |
Genome Damage and Stability Center/ DNA reapir assay/英國 |
|
|
18 |
台大醫院 |
OTC |
Children's National Medical Center/ Allopurinol test/美國 |
|
|
19 |
台大醫院 |
EB |
GeneDx, Inc./ JEB mutation analysis/美國 |
|
|
20 |
台大醫院 |
OTC |
Children's National Medical Center/ Allopurinol test/美國 |
|
|
21 |
台中榮總 |
Persistent hyperinsulinemic hypoglycemia of infancy |
Ambry Genetics USA/ GCK gene
analysis/美國 |
GCK gene no detected/ 97.03.09 |
|
22 |
台中榮總 |
Alstrom syndrome |
Centogene GmbH/ ALMS 1
gene/德國 |
Homozygous deletion of two nucleotides in exon 16 of
the ALMS1 gene/ 97.04.25 |
|
23 |
台大醫院 |
SLO |
Mayo Medical Lab/ SLO screen/美國 |
因家屬尋求醫師第二意見後,診斷有所更改,故家屬決定暫不送檢 |
|
24 |
馬偕醫院 |
Lesch Nyhan syndrome |
Baylor College of Medicine/ HPRT enzyne analysis/美國 |
Lesch Nyhan syndrome / 97.05.16 |
|
25 |
台北榮總 |
Robinow Syndrome |
University Medical Center Nijmegen/ ROR2 gene sequence analysis/荷蘭 |
Normal/97.08.12 |
|
26 |
台大醫院 |
Rett syndrome |
Baylor College of Medicine/ MECP2 deletion analysis/美國 |
No mutation detected/98.01.06 |
|
27 |
馬偕醫院 |
MSUD |
Woman's & Children's Hospital/ branched-chain amino
acids enzyme assay/澳洲 |
|
|
28 |
台大醫院 |
HSP |
Athena Diagnostics / SPG4 gene test/美國 |
Negative/ 97.07.25 |
|
29 |
台大醫院 |
CPT Ia |
The Children's Hospital of Philadelphia/ CPT I enayme assay/美國 |
CPT I deficiency / 97.09.05 |
|
30 |
台大醫院 |
CPT II |
Baylor College of Medicine/ CPT II
enzyme assay /美國 |
|
|
31 |
台大醫院 |
OTC |
Children's National Medical Center/ CPS1/OTC enzyme
test/美國 |
Unclear diagnosis/96.05.12 |
|
32 |
台大醫院 |
Citrullinemia I |
Baylor College of Medicine/ Arginiesuccinate
synthase/美國 |
醫師擬更改送檢項目與機構,決定暫不送檢。 |
|
33 |
台大醫院 |
Multiple carboxylase deficiency |
Prevention Genetics/ HLCS gene sequencing/ 美國 |
Mutation in exon 5&9/ 97.06.05 |
|
34 |
馬偕醫院 |
Carrier of UCD |
Children's National Medical Center/ Allopurinol test/美國 |
個案未決定送檢 |
|
35 |
台大醫院 |
Fatty acid oxidation defects |
Baylor College of Medicine/ Carnitine Palmitoyltransferase II Enzyme Assay/ 美國 |
CPT II deficiency / 97.06.27 |
|
36 |
台大醫院 |
SHFM |
GeneDx, Inc./ TP63 gene analysis/美國 |
Negative/97.08.25 |
|
37 |
台大醫院 |
Tetrahydrobiopterin deficiency |
University Children's Hospital Zürich/
Neurotransmitters analysis; Enzymes (DHPR, PTPS, GTPCH, SR) analysis; DNA
analysis of SR, PTPS and PCD/瑞士 |
Normal/97.09.07 |
|
38 |
台大醫院 |
Tetrahydrobiopterin deficiency |
University Children's Hospital Zürich/
Neurotransmitters analysis; Enzymes (DHPR, PTPS, GTPCH, SR) analysis; DNA
analysis of SR, PTPS and PCD/瑞士 |
Very low neopterin and biopterin/97.09.07 |
|
39 |
台北榮總 |
Bardet-Biedl
syndrome |
Department of Human Genetics/ BBS gene test /德國 |
Negative,但因DNA quality low,需重新再送一次檢體/97.12.10 |
|
40 |
台大醫院 |
Rubinstein-Taybi syndrome |
Chicago Genetic Service Lab/ CREBBP
sequencing/美國 |
建議送柯滄銘婦產科診所 |
|
41 |
台大醫院 |
FSHD |
Athena Diagnostics / FSHD DNA test/美國 |
Negative/ 97.09.19 |
|
42 |
台大醫院 |
Miller-Dieker Syndrome |
University of Chicago Genetic Services Laboratories/ LIS1
mutation analysis/美國 |
Abnormal/97.10.15 |
|
43 |
台中榮總 |
Sulfite Ocidase
deficiency |
Duke University Medical Center/ Sulfite analyte:S-sulfocysteine/美國 |
|
|
44 |
高雄榮總 |
GSD III |
Duke University/GSD III gene test/美國 |
GSD type III/97.11.26 |
|
45 |
高雄長庚 |
Mitochondrial defect |
/Mitochondrial defect( POLG1 gene mutation
analysis)/美國 |
No mutation/98.01.13 |
|
46 |
台北榮總 |
Multiple Sclerosis |
Mayo Medical Lab/ NMO-IgG Serum /美國 |
Negative/97.12.12 |
|
47 |
台大醫院 |
HSP |
Athena Diagnostics / SPG31 SPG3ASPG6 gene test/美國 |
安排送檢中 |
|
48 |
台北榮總 |
Multiple Sclerosis |
Mayo Medical Lab/ NMO-IgG Serum /美國 |
安排送檢中 |
|
49 |
台北榮總 |
Multiple Sclerosis |
Mayo Medical Lab/ NMO-IgG Serum /美國 |
安排送檢中 |
|
50 |
台大醫院 |
CPT II |
Baylor College of Medicine/ carnitine-acylcaritine translocase enzyme activity research test /美國 |
等待審查中 |
|
51 |
台大醫院 |
CF |
Canterbury Health Laboratorues
/Cystic Fibrosis(CF 29 arms assay &DHPLC )/ 紐西蘭 |
建議改送國內彰化基督教醫院 |
|
52 |
台大醫院 |
HSP |
Centogene GmbH / SPG7 gene test/德國 |
等待醫事處出口公文 |
|
53 |
台中榮總 |
OTC |
Children's National Medical Center Laboratory
Medicine/ Allopurinol Test/美國 |
安排送檢中 |
|
54 |
台北馬偕 |
Tyrosinemia type I |
Molecular Diagnostics and BioBanking/ FAH Gene Sequence Analysis/美國 |
等待審查中 |
|
55 |
台大醫院 |
Niemann-Pick type C enzyme
assay |
Women’s and Children’s Hospital/ Niemann-Pick type C enzyme assay /澳洲 |
建議改送國內淡水馬偕醫院 |
|
56 |
台大醫院 |
Rhizomelic
Chondrodysplasia Punctata Type 1 |
Kennedy Krieger
Institute /Genetics Phytanic acid oxidase and RBC plasmalogen content analysis/ 美國 |
Rhizomelic
Chondrodysplasia Punctata Type 1/97.08.22 |
|
57 |
高雄榮總 |
Homozygous familial
hypercholesterolemia |
Universiteit Van Amsterdam/Familial
hypercholesterolemia Homozygous gene test/荷蘭 |
Familial hypercholesterolemia/97.06.23 |
|
58 |
高雄榮總 |
Homozygous familial
hypercholesterolemia |
Universiteit Van Amsterdam/Familial
hypercholesterolemia Homozygous gene test/荷蘭 |
Familial
hypercholesterolemia/97.06.23 |
|
59 |
高雄榮總 |
Homozygous familial hypercholesterolemia |
Universiteit Van Amsterdam/Familial
hypercholesterolemia Homozygous gene test/荷蘭 |
Familial
hypercholesterolemia/97.06.23 |
|
60 |
高雄榮總 |
Homozygous familial
hypercholesterolemia |
Universiteit Van Amsterdam/Familial
hypercholesterolemia Homozygous gene test/荷蘭 |
Familial
hypercholesterolemia/97.06.23 |
|
共服務60人次,補助39案,國民健康局補助581,381元,本會補助621,794元 |
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註(1)表列之個案為本會當年度服務之個案。 註(2)基金會補助之費用統計,含部份患者無能力自付20%部分。 註(3)60案中有5名個案之檢驗費為個案全額自費。 |