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. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Am J Med Genet A. 2012 Sep 10;158A(10):2393–2406. doi: 10.1002/ajmg.a.35561

Table II.

Clinical characteristics of 53 patients with RES.

Pt ID Age Sex GLH Features VACTERL Features Other Brain Malfs Notes
Alo TA CMS Vert SD Cardiac/Renal/GI/GU Limb
RES Without Alopecia or VACTERL (13 patients)
1 10m F - 2/5 - - - -
3 22m F - - 1/5 - - - -
10 26y M - - 0/5 - - - -
11 6y F - - 2/4 - - - - Congenital pyriform aperture stenosis
16 44y F - - 0/5 - - - -
22 7y M - - NA Bilateral microtia, aural atresia, L corneal clouding attributed to infection
23 2y M - - 3/5 - - - -
26 5y F - - 1/5 - - - - Gestational DM
38 13m F - - NA - - - -
40 9y F - - NA - - - - L corneal clouding attributed to scarring from incomplete eye closure, no TA on exam
42 2y F - - NA - - - -
46 15y M - - 2/5 - - - Urachal cyst
47 16y M - - 0/5 - - -
RES with Alopecia (23 patients)
2 3y F L - 3/5 - - - -
14 5y M R - 0/5 - - - Poss MIF-like HPE
17 4y M L - 3/5 - - - -
18 7y F L>R - 3/5 - - - - R squamosal CSO s/p surgery, eyebrow tuft
28 4y M R>L - 2/5 - - - -
41 16m M L - 2/5 - - - -
4 22m M B - 3/4 - - - -
6 5y M B - 2/5 - - - - Gestational DM.
B SN hearing loss.
Chordee.
7 6y F B - 4/5 - - - P PMG B SN hearing loss
9 14y M B - 2/5 - - - -
12 4y M B - 0/3 - - - -
13 2y M B - 3/5 - - - -
24 5y M B - 2/5 - - - - Idiopathic renal failure
25 27m M B - 3/5 - - - - Neurofibromatosis with NF1 mutation
27 2y M B - 3/5 - - - -
31 6y F B - 2/5 - - - -
32 5y M B - 2/5 - - - -
34 4y M B - 3/5 - - - -
39 3y M B - 3/5 - - - Gestational DM
45 4y F B - 3/5 - - - - CSO
48 9y M B - NA - - - - CSO s/p surgery
51 4y F B - NA - - - -
52 3y F B - NA -
RES with Alopecia and Trigeminal Anesthesia (3 patients)
8 3y F B B 4/5 - - - - Multi-suture CSO s/p surgery
44 31y M B B 3/5 - - - - CSO s/p surgery
53 9y F B B NA -
RES with VACTERL Features (+/− Alopecia) (12 patients)
5 5y F B - 4/4 - Duplicated renal collecting system, retro-esophageal cyst Radial aplasia B - TAR syndrome with 1q21.1 deletion
19 6y M R - 1/3 Y ASD, VSD, bicuspid AV Radial aplasia R - Posterior skull defect.
Possible CSO.
20 4y M - - 1/5 - - PPD L hand - Temporal tuft
21 3y M - - NA - Absent R kidney, fused/duplicated L kidney - -
29 17y M R - 0/5 Y Absent L kidney, PUV - - Gestational DM
30 3y M L>R - 4/5 Y Absent L kidney, Hypoplastic AA, VSD - -
33 12y F - - 5/5 Y - - -
36 19m F B 3/5 Y TOF, RSAA, horseshoe kidney -
37 4y F - - NA - TAPVR, anal atresia - -
43 10m F B - 2/5 Y VSD - -
49 23y M - NA - - PPD L hand - Temporal tuft, posterior skull defect
50 5y F NA NA NA NA Absent kidney, body wall defect PPD R foot - Mother with pre-existing DM
RES with Posterior HPE, Aventriculy and VACTERL Features (+/− Alopecia) (2 patients)
15 3y F R - 1/3 Y - - Post HPE, AV Mother with pre-existing DM. Microcephaly.
Forme fruste cleft lip.
35 2d M - NA 2/5 Y TOF Fused/duplicated R hallux Post HPE, AV Mother with pre-existing DM. Microcephaly.
Malformed ears.

Abbreviations: Alo, Alopecia. TA, trigeminal anesthesia. CMS, composite morphology score. DM, diabetes mellitus. MIF, middle interhemispheric fusion [variant of holoprsoencephaly]. HPE, holoprosencephaly. CSO, craniosynostosis. SN [hearing loss], sensorineural. P PMG, perisylvian polymicrogyria. ASD, atrial septal defect, VSD, ventricular septal defect. [Bicuspid] AV, aortic valve. PUV, posterior urethral valves. [hypoplastic] AA, aortic arch. TOF, Tetralogy of Fallot. RSAA, right-sided aortic arch. TAPVR, total anomalous pulmonary venous return.