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Table 3 Details of 22 patients with CAKUT

From: A prospective observational study of associated anomalies in Hirschsprung’s disease

ID

Sex

HSCR type

CAKUT

Side

Other anomalies

1

M

TIA

MCDK

R

 

2

F

TCSA

RH

B

HI

3

M

TCSA

RA

L

FMTC; VI

4

M

TCSA

VUR

B

 

5

M

L-HSCR

RH

R

ONDINE; CRYPTO; VI; HI

6

M

S-HSCR

RH

R

VI

7

M

S-HCSR

DCS

L

VI

8

M

S-HCSR

HN

B

VI

9

M

S-HCSR

HN

L

PALATE CLEFT

10

M

S-HSCR

VUR

R

EAR PIT

11

F

S-HCSR

RH + DCS

B

VI; HI

12

M

S-HCSR

RH

L

VI; HI

13

M

S-HCSR

VUR

B

CAT EYE; CHD; VI; EAR PIT

14

M

S-HSCR

RH

R

VI

15

F

S-HSCR

RH

B

 

16

M

S-HSCR

RH + HN

B

DOWN; CHD; VI

17

M

S-HSCR

VUR

R

 

18

M

S-HSCR

HN

B

VI; DISLESSIA; CCA

19

M

S-HSCR

HN

L

VI

20

M

S-HSCR

VUR + PUV + RH

R

 

21

F

S-HSCR

RH

R

VI

22

M

S-HSCR

VUR

L

DOWN; ATRESIA

  1. Legend: TIA, Total Intestinal Aganglionosis; TCSA, Total colonic aganglionosis; L-HSCR, Aganglionosis extended between left transverse colon and the cecum; S-HSCR, Aganglionosis extending up to the splenic flexure; MCDK, Multicystic Dysplastic Kidney; RH, Renal hypoplasia; RA, Renal Asymmetry; HN, Hydronephrosis; VUR, Vesicoureteric Reflux; DCS, Duplex Collecting System; PUV, Posterior urethral valve; R, Right; B, Bilateral; L, Left; HI, Hearing impairment; FMTC, Familiar Medullary Thyroid Carcinoma; VI, Visual Impairment; CRYPTO, Cryptorchidism; CHD, Congenital Heart Disease; CCA, Corpus Callosum Agenesis.
  2. Sixteen right and 14 left rental units were involved for a slight right side preponderance. Most of HSCR patients with CAKUT (17/22 = 77%) had further associated malformations.