Skip to main content

Table 2 The cases with parental consanguinity

From: Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray

Case #*

Age

Sex

Referring reasons

Size of HZ (Mb)

Estimated coefficient of inbreeding (F)

Post-testing information on mating type

001

6 y

F

ID

598

1/4

Brother-sister

002

3 y

M

DD, DE, DF,RA

839

1/4

No related

003

18 y

M

DD, ID

624

1/4

NA

004

23 d

F

CA

345

1/8

Uncle-niece

005

7 y

M

DD

383

1/8

1st cousins

006

3 d

M

CA

285

1/8

NA

007

9 d

M

SZ

338

1/8

Distantly related

008

12

F

DD, DF

292

1/8

NA

009

12 y

F

SKS, MD

187

1/16

1st cousins

010

9 y

M

SS

196

1/16

1st cousins

011

1 y

M

DD

250

1/16

1st cousins

012

7 y

M

DF, CA, RF

208

1/16

1st cousins

013

3 y

M

DD

139

1/16

NA

014

7 y

F

DD, DF, FT

114

1/32

2nd cousins

015

2 y

F

DD, FT

85

1/32

From the same small town

016

5 y

M

DD

120

1/32

Consanguineous

017

1 m

F

CA

69

1/32

2nd cousins

018

1 y

F

ID, GR, SS

88

1/32

NA

019

6 y

F

DD

86

1/32

2nd cousins

020

18 d

M

DF, MM

72

1/32

NA

021

3 y

F

DD

96

1/32

NA

  1. Abbreviations: CA congenital anomalies, DD developmental delay/disorder, DE diaphragmatic eventration, DF dysmorphic features, FT failure to thrive, GR growth retardation, ID intellectual disability, MD motor delay, MM multiple malformations, NA no information available, RA renal anomalies, RF renal failure, SKS scoliosis and kyphoscoliosis, SS short stature, SZ seizures. *Numbers are used for this publication only, not the real numbers used for patient management.