Meckel's Syndrome

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Identifier walsh_1971_s4_c2
Title Meckel's Syndrome
Creator Rufus Howard
Subject Polycystic Kidney Diseases; Chromosome Disorders; Nervous System Malformations
History Seven cases of the Meckel syndrome occurred in two families.
Pathology Gross congenital abnormalities
Disease/Diagnosis Meckel syndrome
Clinical In 1967 a pair of identical male twins were born with identical severe malformations (encephalocele, bilateral microphthalmia, Polydactyly and polycystic kidneys) and died shortly after birth.
Presenting Symptom Encephalocele; Bilateral microphthalmia; Polydactyly; Polycystic kidneys
Neuroimaging N/A
Treatment N/A
References 1. Meckel, J.F., Dtsch. Arch. Physiol. 7:99-172, 1822. 2. Gruber, G.B., Beitr. Path. Anat. 93:459-476, 1934. 3. Opits, J.N. and Howe, J.J., The Meckel Syndrome. Birth Defects, Original Article Series, 5/2:167-179, Feb. 1969. 4. Miller, J.O. and Selden, R.F., Arhinencephaiy, Encephlocele, and 13-15 Trisomy Syndrome with Normal Chromosomes, Neurology 17:1087-1091, Nov. 1967.
Language eng
Format application/pdf
Type Text
Source 1971 Walsh Proceedings
Relation is Part of Case presented at the NANOS 1972 Walsh Session, February 26-27 Contributor Primary
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights Management Copyright 2008. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6mp5645
Contributor Primary Howard, Rufus
Contributor Secondary Albert, Daniel
Setname ehsl_novel_fbw
ID 178913
Reference URL https://collections.lib.utah.edu/ark:/87278/s6mp5645
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