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

Table 4 Details of HSCR patients with CHD

Pt ID	Sex	Age (m)	HSCR type	Disease	Management	Other anomalies
1	F	12	TCSA	AC	Surgical intervention	TURNER
2	F	291	S-HSCR	ASD + VSD + MI	Surgical intervention	DOWN; CAKUT; VI
3	M	152	S-HSCR	ASD + VSD	Surgical intervention	DOWN; VI
4	M	15	S-HSCR	ASD + VSD	Surgical intervention	CAT EYE; CAKUT; VI; EAR PIT
5	M	3	S-HSCR	ASD + small VSD	F-UP	DOWN
	M	26	S-HSCR	AS DIL.	F-UP	CAKUT; VI
	M	52	L-HSCR	AS DIL.	F-UP	CAKUT; EAR PIT
	M	134	S-HSCR	AS DIL.	F-UP
	M	95	TCSA	ASD (OS)	F-Up
	M	161	S-HSCR	ASD (OS)	F-Up	VI; IPERTG; CRYPTO
	M	288	S-HSCR	ASD (OS)	F-Up	VI; OSTEOPOROSIS
	M	40	S-HSCR	ASD (OS)	F-Up	DOWN

Legend: AC = Aortic Coarctation; ASD = Atrial Septal Defect; VSD = Ventricular Septal Defect; MI = Mitral Insufficiency; F-UP = Follow up; AS DIL. = Aortic Sinus Dilatation.
Five patients were diagnosed with major CHD (4.7%). Four patients required cardiac surgery. All patients with CHD suffered from chromosomal abnormalities (3 Down, 1 Cat Eye, and 1 Turner Syndrome). In addition to the above-mentioned abnormalities, we detected dilatation of the aortic sinus in 3 patients and ostium secundum type ASD in 4. All those patients are being followed up in the long term.

ISSN: 1750-1172