Craniosynostosis: Difference between revisions
Jump to navigation
Jump to search
| Line 65: | Line 65: | ||
<html> | <html> | ||
<div class="card d-flex"> | <div class="card d-flex"> | ||
<div class="card-body" | <div class="card-body" ><video controls="" id="player" style="width: 60%;" poster="https://www.fmichael1.com/moodle/local/VOD_gal/media/youmans8e/VOLUME_2/SECTION_8_Pediatrics/PART_3_Craniosynostosis/Video_220-1_Syndromic_Craniosynostosis.jpg"> | ||
<source src="https://www.fmichael1.com/moodle/local/VOD_gal/media/youmans8e/VOLUME_2/SECTION_8_Pediatrics/PART_3_Craniosynostosis/Video_220-1_Syndromic_Craniosynostosis.mp4" type="video/mp4" /> | <source src="https://www.fmichael1.com/moodle/local/VOD_gal/media/youmans8e/VOLUME_2/SECTION_8_Pediatrics/PART_3_Craniosynostosis/Video_220-1_Syndromic_Craniosynostosis.mp4" type="video/mp4" /> | ||
<track default="" kind="captions" label="English" src="https://www.fmichael1.com/moodle/local/VOD_gal/media/youmans8e/VOLUME_2/SECTION_8_Pediatrics/PART_3_Craniosynostosis/Video_220-1_Syndromic_Craniosynostosis.vtt" srclang="en" /> | <track default="" kind="captions" label="English" src="https://www.fmichael1.com/moodle/local/VOD_gal/media/youmans8e/VOLUME_2/SECTION_8_Pediatrics/PART_3_Craniosynostosis/Video_220-1_Syndromic_Craniosynostosis.vtt" srclang="en" /> | ||
</video | </video> | ||
<script> | <script> | ||
Revision as of 14:32, 3 February 2024
Types of craniosynostosis
Nonsyndromic Craniosynostosis
Single suture craniosynostosis
Pathology
- Bone growth primarily perpendicular to & occurring at suture lines; premature fusion → abnormal growth
Classification of single suture craniosynostosis
Syndromic craniosynostosis
Selected craniofacial dysmorphic syndromes
| Syndrome | Sporadic | Inherited | Craniofacial findings | Associated findings |
|---|---|---|---|---|
| Crouzon Syndrome (craniofacial dysostosis) | Yes (25%) | FGFR2 (AD) | Craniosynostosis of coronal & basal skull sutures, maxillary hypoplasia, shallow orbits, proptosis | HCP rare |
| Apert Syndrome (acrocephalosyndactyly) (MC) | Yes (95%) | FGFR2 (AD) | same as Crouzon | Syndactyly of digits 2, 3, 4; shortened UE, HCP common |
| Kleeblattschädel Syndrome | Yes | AD | Craniosynostosis /w trilobular skull | isolated, or with Apert's or thanatophoric dwarfism |
Youmans Video - Video 220-1 Syndromic Craniosynostosis