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. 2014 Jan 28;7:10. doi: 10.1186/1755-8166-7-10

Table 2.

Major clinical findings for all three reported patients

  Case 1 (14 years) Case 2 (21 years) Case 3 (19 years)
 
- two spontaneous abortions
- male twin: facial dysmorphism severe early delay; death at 18 months of age
 
 
- one maternal uncle with ID
- one brother: facial dysmorphism severe developmental delay, seizures, autistic features, death at 23 years of age
 
Physical data
(at birth)
 
 
 
GW
40
39
40
L (cm)
49 (50 pc)
Not known
51 (50 pc)
BW (g)
2400 (10 pc)
3000 (50 pc)
3780 (75 pc)
HC (cm)
36 (50 pc)
Not known35
(50 pc)
Early development
Walking (months)
18
13
15
Speech onset (years)
5 (few words) → 12 (fair)
4
3
Behaviour
Difficulty of separation and isolation
Hyperactivity
Tantrum
School age
Neurological condition
Normal
Normal
Normal
Learning
Difficulties
Difficulties
Difficulties
Intelligence
Moderate (IQ 41)
Borderline (IQ NA)
Borderline (IQ 80 when 6 years)
Communication/social conduct
Difficulties
Good
Difficulties (since 3 years)
Behaviour
Quiet and withdrawn
Hyperactivity, attention deficit, impulsiveness
Hyperactivity
Adolescence
Neurological condition
 
 
 
Motor coordination
Fair
Poor
Fair
Hypotonia/joint laxity
Yes
Yes
Yes
Intelligence
Scarce (IQ NA)
Borderline (IQ 84 when15 years)
Mild (IQ 57 when17 years)
Communication/social conduct
Difficulties
Difficulties
Difficulties
Behaviour
Quiet and meek
Hyperactive, anxious, mood disorder
Anxious, depressive mood
Dysmorphic features
Minor facial dymorphisms (broad nasal bridge, prognatism, mild ocular hypertelorism)
Minor facial dysmorphisms (broad nasal bridge, prognatism)
None
Diagnostics
EEG
Normal
NA
Posterior slow waves
MRI Normal NA Normal

GW: gestational age; L: length; BW: body weight; HC: head circumference; IQ: intelligence quotient (ascertained according to WISC-R scale); ID: intellectual disability; NA: not ascertained.