Table 2 Syndrome/conditions associated with infantile inguinal hernia
From: The demographic profile and the management of infantile inguinal hernia: a 3-year’s review
No of study subjects-118 | GI-(0–6 months) N-89 | GII (6–12 months) N-29 |
|---|---|---|
Isolated syndromic | 2 (2.24%) DS-1 (1.12%) CL-1 (1.12%) | 0 |
Syndromic asso with other cong anomalies | 2 (2.24%) *Edward syndrome + CTEV + webbed neck -1 (1.12%) *Edwards syndrome + RDS-1 (1.12%) | 1 (3.44%) *CL + HUN + Pectus excavatum |
Non syndromic Conditions | 19 (21.34%) *Gerd-2 *Sept arthritis-1 *BLHN-1 *UDT-2 *UH-3 *HYPO-2 *ROP-1 *CHD-2 *SLOL-1 *CLEFT PL-1 *Cong cataract-1 *DDH-1 *EHBA-1 *Duplicated extrophy-1 | 9 (31%) *EEC + Cervical MMC + Spina bifida + Small Phallus *Chylous Ascites-1 *CHD-3 *GDD + Spastic Diplegia-1 *LIMB anomalies-1 *UDT-2 |
Other surgeries | 7 (7.8%) *Orchidopexy-2 (2.24%) *Circumcision-1 *Arthrotomy-1 *Cataract surgery (IOL)-1 *Kasai’s procedure-1 *Excision of duplicated Extrophy-1 | 5 (17.24%) *Orchidopexy-2 (6.8%) *Circumcision-1 *EEC + MMC repair-1 |