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Table 1 Comparison of the clinical findings in patients with parital trisomy 4q

From: Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array

 

Taylor et al. [13]

Stoll et al. [14]

Mikelsaar et al. [15]

Lundin et al. [16]

Rinaldi et al. [17]

Lin et al. [18]

Egritas et al. [19]

Velinov et al. [20]

Cakmak−Genc et al. [21]

White et al. [22]

Our study

 

Case 1

Case 2

Duplication region

4q26-q35

4q26-qter

4q25-qter

4q27-q35

4q24-q35

4q28.1-q35

4q25-qter

4q25-qter

4q28-qter

4q24-qter

4q28.3-qter

4q28.3-qter

Deletion region

21q21.1-q22.3

9p24-pter

Xq22-qter

Xp21.3-p22.33

6p25.2-p25.3

Age/Sex

6.5/M

11/F

7/F

13/F

1/M

2.5/M

1.25/F

NB/F

NB/F

32/F

28/F

Fetus

Growth retardation

 + 

 + 

 + 

 + 

 + 

 + 

 + 

NM

IUGR

Intellectual disability

 + 

 + 

 + 

 + 

 + 

 + 

NM

 + 

NA

Microcephaly

 + 

 + 

 + 

 + 

 + 

 + 

 + 

NA

Low−set/malformed ears

 + 

 + 

 + 

 + 

 + 

 + 

 + 

 + 

NA

Retrognathia/micrognathia

NM

NM

 + 

 + 

 

 + 

NA

High/broad nasal bridge

 + 

 + 

 + 

 + 

 + 

 + 

NM

 + 

 + 

NA

Thumb anomalies

NM

 + 

 + 

 + 

NM

NA

Epicanthic folds

NM

NM

NM

 + 

NM

 + 

 + 

NM

NA

Congenital heart defect

 + 

NM

 + 

NM

 + 

 + 

 + 

Renal hypoplasia

NM

NM

 + 

NM

NA

Epilepsy

 + 

NM

NM

NM

NM

 + 

NA

Other

 

Factor X defect

   

Choanal-atresia

Cholestasis

 

Choanal-atresia

Secondary amenorrhea

Short stature

 
  1. −:absent; +: present, NA not applicable, NB new born, NM not mention, F female, M male, IUGR intrauterine growth restriction