Skip to main content

Table 3 Associated disorders and anomalies according to the parental origin of the retained X chromosome

From: Effect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome

Type

Cardiac anomalies

Renal anomalies

Webbed neck

Ear disorders

Thyroid disorders

Parental origin

Xm

Xp

Xm

Xp

Xm

Xp

Xm

Xp

Xm

Xp

A/T: (%);

18/67a (26.9)

8/26a (30.8)

16/67b (23.9)

6/26b (23.1)

23/67b (34.3)

9/26b (34.6)

31/67c (46.2)

12/26c (46.1)

14/67d (21)

6/26d (23.1)

  1. A/T: affected/total (%); Fisher’s exact test: ap =  0.7980; bp =  1.0, cp =  0.1547; dp =  0.7862.