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. 2015 Dec 16;24(8):1112–1116. doi: 10.1038/ejhg.2015.264

Table 1. Clinical features of eight ACAD9 patients.

  Patient 1 Patient 2 Patient 3 Patient 4 Patient 5 Patient 6 Patient 7 Patient 8
Clinical features                
 Gender M F F M F M F F
 Affected relatives One brothera (H6) 1a in utero 1 brothera at birth (CH) 1 sistera at birth 1 sistera (5 mo)
 Age at first symptoms Neonatal Neonatal 12 m 18 m 9 y 4 m 15 m 12 m
 Current age aH11 a71 d a6 y 15 y 35 y 22 y a21 m a18 m
 
Early cardiac symptoms
  Cardiac hypertrophy + + + + + + + +
  Heart transplantation 2 y 9 y 18 y
 
Delayed neurological symptoms
  Cognitive impairment nr nr + +
  Seizures nr nr +
  Brain MRI nd leucodystrophy nd nd N at 14 y nd N
 Other organ involvement Liver failure Exercise intolerance Tubulopathy Exercise intolerance Tubulopathy, POF Optic atrophy
 
Laboratory
 Plasma lactate (mmol/l) 20 >3 7,4 6,4 4 >3 8 5,5–14
 
Complex I deficiency
  Heart N Severe Mild Severe Mild Severe Severe  
  Muscle Severe Severe Mild Severe Severe N   Severe
  Fibroblasts Mild N N N N N nd Mild
 Nucleotide change c.1249C>Tc.1030–1G>T c.2T>Gc.1015T >G c.358delTc.1594C>T c.976G>Cc.1595G>A c.151-2A>Gc.1298G>A c.1237G>Ac.1552C>T c.1552C>Tc.1564-6_1569del c.1 A >Gc.796C>T
 Aminoacid change p.(Arg417Cys)acceptor splice site p.(Met1?)p.(Phe339Val) p.(Phe120Serfs*9)p.(Arg532Trp) p.(Ala326Pro)p.(Arg532Gln) acceptor splice sitep.(Arg433Gln) p.(Glu413Lys)p.(Arg518Cys) p.(Arg518Cys)splice site p.(Met1?)p.(Arg266Trp)

Abbreviations: CH, cardiac hypertrophy; d, day; NA, not applicable; nr, not relevant; N, normal; nd, not done; m, month; POF: premature ovarian failure; w, week, y, year.

a

Deceased. ACAD9 reference sequence is NM_014049.4.