Phenotypes for disease #01849 (NAGSD (deficiency, N-acetylglutamate synthase (NAGSD)), OMIM:237310)

51 entries on 1 page. Showing entries 1 - 51.
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Individual ID     
0000045124 vomiting, poor feeding, episodic confusion as neonate - - Unknown - 00y06m - - - Johannes Häberle 00058532
0000045172 transient coma at y5 - - Unknown 33y - - - - Johannes Häberle 00058577
0000045173 hypotonia at 2.5m, later hepatomegaly, failure to thrive, hyperammonemia - - Unknown - - - - - Johannes Häberle 00058578
0000045174 hypotonia, developmental delay - - Unknown - - 00y03m - - Johannes Häberle 00058579
0000045175 heterozygous mutation reported in a control sample. No further information - - Unknown - - - - - Johannes Häberle 00058580
0000045176 neonatal hyperammonemia - - Unknown - - 00y00m01d - - Johannes Häberle 00058581
0000045177 vomitting, failure to thrive, hepatomegaly, recurrent asymptomatic hyperammonemia, normal at y5 with benzoate, citrulline and protein restriction - - Unknown - - 00y00m20d - - Johannes Häberle 00058582
0000045178 vomitting, hypotonia, somnolence at 24y normal cognitive function NCG-treated - - Unknown - - 00y13m - - Johannes Häberle 00058583
0000045179 late-onset and mild course Normal outcome without NCG - - Unknown - - - - - Johannes Häberle 00058584
0000045180 onset at y27, during pregnancy, with seizures and coma - - Unknown - - 27y - - Johannes Häberle 00058585
0000045181 late-onset with migraine, nausea, vomitting, lethargy, ataxia and coma normal at 57y - - Unknown - - 40y - - Johannes Häberle 00058586
0000045182 severe hyperammonemia stable at 6m with NCG treatment, death after stopping NCG elder brother died at 2y (no material or diagnosis) - - Unknown - - 00y02m - - Johannes Häberle 00058587
0000045183 UTI, somnolence, decreased conscience, peak ammonia 350 umol/l normal outcome - - Unknown - - 15y - - Johannes Häberle 00058588
0000045185 Hyperammonemia, NH3=203 umol/l, presenting at age 10y; no mental retardation - - Familial - - - - - Nicholas Ah Mew 00058590
0000045188 atypically late onset of hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058593
0000045191 neonatally fatal hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058596
0000045192 died in neonatal period with hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058597
0000045193 died from hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058598
0000045194 acute neonatal hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058599
0000045198 died from neonatal hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058603
0000045199 died neonatal hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058604
0000045200 died from neonatal hyperammonemia - - Unknown - - - - - Johan den Dunnen 00058605
0000046706 poor feeding, seizures, lethargy younger sibling: NCG-treated before symptoms developed - - Unknown - - 00y00m02d - - Johannes Häberle 00060216
0000046707 vomiting, lethargy, no NCG - - Unknown - - 00y00m03d - - Johannes Häberle 00060217
0000046708 poor feeding, somnolence, seizures, normal psychomotor development at 2.5y younger sibling: NCG-treated before symptoms developed - - Unknown - - 00y00m02d - - Johannes Häberle 00060218
0000046709 neonatal onset died at d5 with hyperammonemia - - Unknown - - - - - Johannes Häberle 00060219
0000046710 vomiting, irritability, lethargy, many hyperammonemic episodes, normal cognitive development Sibling: onset at 9y, lethargy, anorexia, vomiting, seizures - - Unknown - 18y 00y01m - - Johannes Häberle 00060220
0000046711 Reye-like syndrome at 16y with hyperammonemia normal outcome - - Unknown - - - - - Johannes Häberle 00060221
0000046712 hypotonia, poor feeding, lethargy - - Unknown - - 00y00m02d - - Johannes Häberle 00060222
0000046713 convulsions and microcephaly at 4y - - Unknown - 04y - - - Johannes Häberle 00060223
0000046714 neonatal death with hyperammonemic coma - - Unknown - - 00y00m01d - - Johannes Häberle 00060224
0000046715 hyperammonemic coma - - Unknown - - 00y00m01d - - Johannes Häberle 00060225
0000046716 hyperammonemic encephalopathy - - Unknown - - 00y00m03d - - Johannes Häberle 00060226
0000046717 hyperammonemic coma, death on 7d sibling: neonatal onset, hyperammonemic coma, death on 19d - - Unknown - - 00y00m01d - - Johannes Häberle 00060227
0000046718 treated but unstable until NCG started at 36m, suffers neurological sequelae Sibling: prospective treatment from birth, but NCG only started at 3m, suffers neurological sequelae - - Unknown - - 00y00m04d - - Johannes Häberle 00060228
0000187293 see paper; … NAGS deficiency NAGSD Familial, autosomal recessive - - - - - Johan den Dunnen 00248284
0000187305 2d-hyperammonemia requiring dialysis; alive under treatment including NCG - NAGSD Familial, autosomal recessive - - 00y00m02d - - Johan den Dunnen 00248296
0000187306 Index: 2d-vomiting, feeding problems, hyperammonemia was diagnosed and treated with hemodiafiltration; 1y-normal development under treatment with NCG Elder sibling: onset first few days, death in early neonatal period, no ammoniameasurements done - NAGSD Familial, autosomal recessive - - - - - Johan den Dunnen 00248297
0000187307 neonatal onset with hyperammonemia (max. 368 μmol/L), metabolically stable with NCG - - Unknown - - - - - Johan den Dunnen 00248298
0000187308 Index: 4d-onset; 22d-death hyperammonemic encephalopathy: Sibling: 2d-onset, treated but unstable until NCG started at 3m; 13y-normal neurological status - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248299
0000187309 1d-onset; 4d-death - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248300
0000187310 Index: 2d-onset; 8m-liver transplantation, no information on neurological status: Sibling: 2d-onset - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248301
0000187311 2d-onset, hyperammonemic encephalopathy; 4d-death with cerebral edema - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248302
0000187312 neonatal onset - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248303
0000187313 6d-onset, poor feeding, lethargy; 3m-death - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248304
0000187314 Index: 3d-onset hyperammonemic coma; 6m-death: Sibling and relative: genetic demonstration and NCG treated before symptoms developed - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248305
0000187315 2d-onset, poor feeding, seizures; psychomotor delay and spasticity, NCG treatment - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248306
0000187316 neonatal onset with hyperammonemia - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248307
0000187317 3d-onset, standard treatment for hyperammonemia without NCG; 22m-alive while treated - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248308
0000187318 neonatal onset with hyperammonemia - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248309
0000187319 1m-hyperammonemia; 22m-diagnosed while under treatment with diet and NCG - NAGSD Familial, autosomal recessive - - - - - Johannes Häberle 00248310
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