Table 1 Summary of the clinical features of patientsa

From: A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder

 

Submicroscopic deletions involving MEIS2

Nucleotide alterations in MEIS2

Present patient

Number of the patients

12

2

 

Developmental delay

10/12

2/2

+

Verbal developmental delay

2/12

2/2

+

Motor developmental delay

9/12

2/2

+

Autism spectrum disorder

1/12

1/2

+

Congenital heart defects

6/12

2/2

+

Cleft palate

10/12

2/2

+

Gastroesophageal reflux

0/12

2/2

−

  1. Abbreviation
  2. MEIS2, Meis homeobox 2.
  3. a Table 1 reported by Fujita et al.2 is modified.
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