![Page 1: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/1.jpg)
3
![Page 2: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/2.jpg)
autosomal recessive disease
deficiency of glutaryl-CoA dehydrogenase
1 : 100 000 GCDH gene chromosome 19p13.2
![Page 3: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/3.jpg)
![Page 4: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/4.jpg)
![Page 5: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/5.jpg)
#1 The accurate diagnosis of GA-I has important practical implications when devising treatment plans and giving appropriate information to children and their families.
#2 For mass newborn screening for glutaric aciduria type I determination of C5DC in DBS by MS/MS should be used
![Page 6: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/6.jpg)
High excretors:
Amish Lumbee Irish Travellers
Low excretors:
Oji-Cree natives
![Page 7: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/7.jpg)
#3 In a cohort with a high disease incidence due to a single
common GCDH mutation and a low excretor phenotype,
DNA based methods should be considered for newborn
screening. The use of MS/MS-based screening in such
populations will likely lead to false negative results
![Page 8: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/8.jpg)
![Page 9: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/9.jpg)
# 4: For the confirmation of a positive newborn screening result, a specific diagnostic workupis required, including a quantitative analysis of GAand 3-OH-GA
RT: 5.85 - 20.27
6 7 8 9 10 11 12 13 14 15 16 17 18 19 20Time (min)
0
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
Rela
tive A
bundance
8.99
16.60
14.68
17.00
14.1712.20
16.528.70 19.23
10.46 15.948.6719.14
16.16
10.1314.9113.41 18.74
6.88 13.69 15.527.78 9.44 17.12 17.9611.45 18.4112.48 19.2813.196.96 8.19 11.31 17.267.186.846.18 7.39
NL:3.43E8TIC F: MS 165_GAJOVA_Alzbeta
![Page 10: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/10.jpg)
#5 …….GCDH gene mutation analysis, and/or enzyme analysis
#6 Metabolic treatment ……. by an interdisciplinary team….. (metabolic pediatrian, dietetist, nurse) + parents and patients training
#7 low lysine diet
#8. L-Carnitine
#9. Emergency treatment
![Page 11: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/11.jpg)
#9. Emergency treatment should start withoutdelay and should be performed aggressively duringfebrile illness, surgery and immunization within thevulnerable period for acute encephalopathic crises (upto age 6 years)
#10 > 6 years …..
![Page 12: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/12.jpg)
![Page 13: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/13.jpg)
![Page 14: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/14.jpg)
#15. Glutaric aciduria type I should be excluded in children with suspected shaken baby syndrome
#14. Children with subdural haemorrhage and/or bitemporal arachnoid cysts should be investigated for glutaric aciduria
GA I ?
GAI ?
![Page 15: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/15.jpg)
#16 neurosorgical interventions - pediatric neurosurgeon
#17 monitoring in any age, in case of new complications
#18 Urine analysis of GA and 3-OH-GA is not informative for therapy monitoring
![Page 16: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/16.jpg)
![Page 17: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/17.jpg)
Děkuji za pozornostDěkuji za pozornost
![Page 18: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/18.jpg)
![Page 19: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/19.jpg)
![Page 20: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/20.jpg)
![Page 21: 3. autosomal recessive disease deficiency of glutaryl-CoA dehydrogenase 1 : 100 000 GCDH gene chromosome 19p13.2](https://reader035.vdocument.in/reader035/viewer/2022070410/56649f185503460f94c2f020/html5/thumbnails/21.jpg)