Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here for FREE ACCESS to this landmark database

Sign In to gain access to subscriptions and/or personal tools.
Clinical Pediatrics
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
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 Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Iannetti, P.
Right arrow Articles by Guardalà, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Iannetti, P.
Right arrow Articles by Guardalà, C.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Holoprosencephalic Disorders

Case Report of a Semilobar Type

Paola Iannetti

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Luciana Chessa

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Lucilla Brattoli

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Luigi M. Fantozzi

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Luigi Bozzao

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Vincenzo Colloridi

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

Clelia Guardalà

Departments of Pediatrics, Medical Genetics, and Neuroradiology, University 'La Sapienza', Roma, Italy

A child with microcephaly, facial dysmorphisms, seizures, and congenital car diopathy is presented. On the basis of skull x-rays, electroencephalogram, trans- illumination of the head, and computed tomography (CT) scan, the diagnosis of semilobar holoprosencephaly was made. The heterogeneous etiology of the disorder is discussed in order to evaluate the recurrence risk. The usefulness of CT scan for the classification in the different types of holoprosencephaly is stressed.

Clinical Pediatrics, Vol. 23, No. 5, 294-296 (1984)
DOI: 10.1177/000992288402300513
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
 J Child NeurolHome page
R. W. Leech and R. M. Shuman
Midline Telencephalic Dysgenesis: Report of Three Cases
J Child Neurol, July 1, 1986; 1(3): 224 - 232.
[Abstract] [PDF]

Home page
 J Child NeurolHome page
R. W. Leech and R. M. Shuman
Review Article: Holoprosencephaly and Related Midline Cerebral Anomalies: A Review
J Child Neurol, January 1, 1986; 1(1): 3 - 18.
[Abstract] [PDF]