Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-19T10:08:25.816Z Has data issue: false hasContentIssue false

15 - Skeletal Abnormalities

Published online by Cambridge University Press:  23 February 2010

Enid Gilbert-Barness
Affiliation:
University of South Florida and University of Wisconsin Medical School
Diane Debich-Spicer
Affiliation:
University of South Florida
John M. Opitz
Affiliation:
University of Utah
Get access

Summary

OSTEOCHONDRODYSPLASIAS

Bone is formed from collagen. Bone dysplasias predominantly involve one type of collagen (Figure 15.1). Terms used in the description of bone dysplasias according to the defect in collagen are shown in Table 15.1.

The normal growth plate or physis consists of four zones:

  1. resting cartilage;

  2. proliferative cartilage;

  3. hypertrophic cartilage;

  4. zone of provisional calcification.

The revised international classification of osteochondrodysplasias encompasses those disorders that are perinatally lethal and/or amenable to prenatal diagnosis (Table 15.2). Prenatal diagnosis has been made in most of the lethal forms of ostechondrodysplasia (Table 15.3). The osteochondrodysplasias include the infant or fetus with dwarfism. Most are lethal. For most convenience in diagnosis they can be divided into the following groups:

  1. ■ Osteochondrodysplasias with platyspondyly

  2. ■ Osteochondrodysplasias with short trunk

  3. ■ Short rib osteochondrodysplasias

  4. ■ Osteochondrodysplasias with defective bone density

  5. ■ Miscellaneous group

Osteochondrodysplasias with Platyspondyly (Table 15.4)

Although the trunk of the infants in this group is not significantly short, the vertebral bodies in the radiograph are markedly flattened. Histopathologically the physeal growth zones are usually disorganized and may be retarded, but the resting cartilage is mostly unremarkable.

Type
Chapter
Information
Embryo and Fetal Pathology
Color Atlas with Ultrasound Correlation
, pp. 388 - 427
Publisher: Cambridge University Press
Print publication year: 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×