All individuals with variants in gene ECHS1

15 entries on 1 page. Showing entries 1 - 15.
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00050476 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) F - United Kingdom (Great Britain) - - - Decipher - ? clinodactyly of the 5th finger, specific learning disability, joint hypermobility, lumbar hyperlordosis, gingival overgrowth 1 2 Johan den Dunnen
00306141 ECHS1_F1_M PubMed: Abdenur 2020, Journal: Abdenur 2020 Family, healthy homozygous mother F no United States Samoa >45y - - None Healthy/Control Healthy Mother 1 6 Mariella Simon
00306145 ECHS1_F1_F PubMed: Abdenur 2020, Journal: Abdenur 2020 Healthy Carrier Father M no United States white, Portugal >45y - - None Healthy/Control Healthy carrier father 1 1 Mariella Simon
00306146 ECHS1_F1_P1 PubMed: Abdenur 2020, Journal: Abdenur 2020 family, more mildly affected son M no United States Samoa, white, Portugal >16y - - Low Valine Diet ECHS1D 6M-regression 2Y metabolic decompensation with lactic acidosis and ketosis MRI-Leigh's disease milder clinical course than his brothers 14Y decreased vision and intermittent nystagmus,wheelchair bound slurred speech and drooling joint contractures 2 1 Mariella Simon
00306147 ECHS1_F1_P2 PubMed: Abdenur 2020, Journal: Abdenur 2020 family, severely affected, multiple decompensations M no United States Samoa, white, Portugal 09y - - - ECHS1D Suspected Mitochondrial Disease Died before dx was made Regression after multiple decompensations, Leigh Syndrome 2 1 Mariella Simon
00306148 ECHS1_F1_U PubMed: Abdenur 2020, Journal: Abdenur 2020 family, unaffected brother M no United States Samoa, white, Portugal >14y - - - Healthy/Control - 1 1 Mariella Simon
00306149 ECHS1_F1_P3 PubMed: Abdenur 2020, Journal: Abdenur 2020 family, severely affected brother M no United States Samoan, white, Portuguese, >06y - - Low Valine Diet ECHS1D hypertonicity MRI-Leigh syndrome developmental delay recurrent metabolic crises with acidosis and ketosis truncal hypotonia hypertonia in extremities non-ambulatory nystagmus dysphagia 2 1 Mariella Simon
00306150 ECHS1_F2_P - Severely affected patient F no United States Samoan, white, Portuguese,Chinese, Phillipino, Native American >08y - - - ECHS1D regression metabolic decompensations nystagmus MRI-Leigh syndrome truncal hypotonia, hypertonia in extremities lactic acidosis non ambulatory 2 1 Mariella Simon
00306151 family PubMed: Peters 2014 2-generation family, affected sister/brother, unaffected heterozygous carrier parents F;M no Greece - - - - - LS see paper; ..., fatal Leigh disease, increased excretion of S-(2-carboxypropyl)cysteine and several other metabolites 2 2 Johan den Dunnen
00306171 patient PubMed: Sakai 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Japan - - - - - LS see paper; ... 2 1 Johan den Dunnen
00306172 FamPatIII2/3 PubMed: Yamada 2015 3-generation family, affected sister/brother, unaffected heterozygous carrier parents/relatives F;M no Japan - - - - - LS see paper; ... 2 2 Johan den Dunnen
00306173 patient PubMed: Wu 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents M - China - - - - - ? see paper; ... 2 1 Johan den Dunnen
00451705 - - - - - - - - - - - ECHS1D - 2 1 Min Peng
00451706 - - - - - - - - - - - ECHS1D - 2 1 Min Peng
00464299 R142 - - F no China Chinese - - - - ID Progressive intellectual and motor regression, lactic acidosis, elevated blood ammonia, and abnormal signals in the basal ganglia and brainstem bilaterally. 1 2 Xiaomei Luo
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