Abstract
Joubert syndrome (JS) and related disorders (JSRD) are rare autosomal recessive disorders typified by a distinctive cerebellar and brainstem malformation. The diagnosis of JSRD requires the neuroradiological " molar tooth sign" found on magnetic resonance imaging. Many children affected with the disorder die in infancy before diagnosis. Rare diseases or syndromes can pose unique challenges for primary care providers who participate in the day-to-day care of chronically ill and physically and mentally challenged children. This article discusses JS and JSRD to provide insight for primary care providers caring for these special children and adults.
Original language | English (US) |
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Pages (from-to) | 316-322 |
Number of pages | 7 |
Journal | Journal for Nurse Practitioners |
Volume | 8 |
Issue number | 4 |
DOIs | |
State | Published - Apr 2012 |
Externally published | Yes |
Keywords
- Developmental delay
- Genetic disorder
- Joubert syndrome
- Joubert syndrome related disorders
- Molar tooth sign
ASJC Scopus subject areas
- Advanced and Specialized Nursing