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©2011 Baishideng Publishing Group Co.
World J Gastroenterol. Oct 7, 2011; 17(37): 4247-4250
Published online Oct 7, 2011. doi: 10.3748/wjg.v17.i37.4247
Published online Oct 7, 2011. doi: 10.3748/wjg.v17.i37.4247
Exocrine pancreatic insufficiency[1,3-5] |
Hypoplasia/aplasia of alae nasi[1,4,6-8] |
Scalp defect /aplasia cutis[1,6,8] |
Sensory neural hearing loss[1,3,8,9] |
Bilateral cystic dilation of cochlea, low set ears, and temporal bone defect[10] |
Growth retardation, short stature[1,11] |
Dental anomalies: oligodontia and absence of permanent teeth[1,6,7,11] |
Anorectal anomalies: imperforate anus[4,11,12] |
Hypotonia, microcephaly, and mental retardation sometimes normal intelligence[3,7,11] |
lacrimal duct anomalies, coloboma of the lids, superior puncta absence, lacrimal cutaneous fistula, and congenital cataract[13] |
Abnormal frontal hair pattern (upsweep)[7] |
Vesicoureteric reflux, hypospadia, and duplex of uterine and vagina[8] |
Congenital heart diseases such as myxomatous mitral valve, PDA, VSD, ASD, dextrocardia, complex congenital heart disease, and cardiomyopathy[13,14] |
Cholestatic liver disease (one case)[15] |
Café au lait spots[16] |
Hypothyroidism[1] |
Growth hormone deficiency[5] |
Hypopituitarism[17] |
Impaired glucagon secretion response to insulin induced hypoglycemia[18] |
Diabetes mellitus[19,20] |
- Citation: Almashraki N, Abdulnabee MZ, Sukalo M, Alrajoudi A, Sharafadeen I, Zenker M. Johanson-Blizzard syndrome. World J Gastroenterol 2011; 17(37): 4247-4250
- URL: https://www.wjgnet.com/1007-9327/full/v17/i37/4247.htm
- DOI: https://dx.doi.org/10.3748/wjg.v17.i37.4247