help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Journal of Clinical Endocrinology & Metabolism Vol. 15, No. 6 668-679
doi:10.1210/jcem-15-6-668
Copyright © 1955 by the Endocrine Society.
This Article
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Reprints, Permissions and Rights
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McGIRR, E. M.
Right arrow Articles by HUTCHISON, J. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McGIRR, E. M.
Right arrow Articles by HUTCHISON, J. H.

DYSGENESIS OF THE THYROID GLAND AS A CAUSE OF CRETINISM AND JUVENILE MYXEDEMA

E. M. McGIRR, M.B., M.R.C.P. and JAMES H. HUTCHISON, M.D., F.R.C.P.

The University Department of Medicine, Royal Infirmary Glasgow, Scotland
The University Department of Child Health, Royal Hospital for Sick Children Glasgow, Scotland

IN 1888 the Committee appointed by the Clinical Society of London (1) to study myxedema concluded that the disease described under the name of myxedema, as observed in adults, was practically the same disease as that named sporadic cretinism when affecting children. The Committee noted that although these conditions appeared to depend on, or to be associated with, destruction or loss of function of the thyroid gland, the ultimate cause of such destruction or loss was not evident. It would be equally true today to say that the ultimate cause of most cases of either adult or childhood myxedema or of sporadic cretinism, remains obscure. Obvious exceptions are: i) the hypothyroidism which follows accidental ingestion or therapeutic use of goitrogenic substances, including drugs; ii) endemic cretinism, which is usually goitrous and is due to lack of iodine; and iii) sporadic goitrous cretinism, which is usually familial and is probably due to an inborn error of metabolism, genetically transmitted (2, 3).

Received October 9, 1954.




This article has been cited by other articles:


Home page
Arch Pediatr Adolesc MedHome page
M. Kaplan, R. Kauli, U. Raviv, E. Lubin, and Z. Laron
Hypothyroidism Due to Ectopy in Siblings
Arch Pediatr Adolesc Med, November 1, 1977; 131(11): 1264 - 1265.
[Abstract] [PDF]


Home page
Arch Pediatr Adolesc MedHome page
S. W. WRIGHT, G. TARJAN, R. W. LIPPMAN, and T. L. PERRY
Etiologic Factors in Mental Deficiency: Errors of Metabolism That May Lead to Mental Deficiency
Arch Pediatr Adolesc Med, May 1, 1958; 95(5): 541 - 562.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1955 by The Endocrine Society