Identifier |
walsh_1971_s4_c2 |
Title |
Meckel's Syndrome |
Creator |
Rufus Howard, MD; Daniel Albert, MD |
Affiliation |
(RH) New Haven, CT; (DA) Portland, OR |
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 |
Date |
1971 |
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 |
1972 Walsh Session, February 26-27 |
Collection |
Neuro-Ophthalmology Virtual Education Library: Walsh Session Annual Meeting Archives: https://novel.utah.edu/Walsh/ |
Publisher |
North American Neuro-Ophthalmology Society |
Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
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 |
Setname |
ehsl_novel_fbw |
ID |
178913 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6mp5645 |