Deletion syndrome 22q13: what the dentist should know to manage children with Phelan-McDermid syndrome effectively.

Abstract

Deletion Syndrome 22q13 (or Phelan-McDermid Syndrome) is a very rare genetic disorder characterized by general neonatal hypotonia, absent to delayed speech, and global developmental delays. With only 600 cases reported worldwide, the disease remains largely under-diagnosed, but diagnosis is on the rise. Current thinking suggests that 22q13 Deletion Syndrome may be one of the principal causes of idiopathic mental retardation. Patients with Phelan-McDermid Syndrome, especially children, can be a challenge for dental professionals, as it is often associated with autism. Dentists see patients with all kinds of special needs, developmental conditions and disabilities. Children with Phelan-McDermid Syndrome need dental care just like every other child. As with other autism-related disorders, children with Phelan-McDermid Syndrome need sameness and continuity in their environment. The dental literature, however, offers very little information to aid the dentist in the management of these children. This article aims to make dentists aware of the disorder and provides tips and recommendations that dentists may find helpful to manage Phelan-McDermid children more effectively.

• Authors: Chris Ivanoff, Athena E Ivanoff
• Journal: The Journal of the Tennessee Dental Association (J Tenn Dent Assoc) 2014 Spring-Summer Vol. 94 Issue 1 Pg. 15-8; quiz 19-20 ISSN: 0040-3385 [Print] United States
• PMID: 25241497 (Publication Type: Journal Article)

Topics

• Child
• Child Behavior
• Chromosome Deletion
• Chromosome Disorders (complications, physiopathology, psychology)
• Chromosomes, Human, Pair 22
• Cooperative Behavior
• Dental Care for Children
• Dental Care for Disabled
• Dentist-Patient Relations
• Humans
• Mouth Diseases (prevention & control)
• Patient Care Planning
• Patient Care Team
• Tooth Diseases (prevention & control)