Health Dictionary
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Progeria secondary prevention
Introduction
Overview
Overview
Effective measures for the secondary prevention of Hutchinson-Gilford progeria syndrome (HGPS) include nutritional assessment, assessment of the cardiac and neurologic status of the patient, musculoskeletal issues assessment, dental evaluation, ophthalmology evaluation, and audiology evaluation.
Secondary Prevention
Secondary Prevention
Effective measures for the secondary prevention of Hutchinson-Gilford progeria syndrome (HGPS) include:[1]
Cardiac assessment
- In patients with Hutchinson-Gilford progeria syndrome (HGPS) accelerated progressive atherosclerosis is primary concern, so yearly cardiac evaluation should be considered with the following:[2][3][4]
- Electrocardiogram (ECG)
- Blood pressure measurement
- Lipid profile testing
- Echocardiography
Growth management
- A complete nutritional assessment which includes weight/height on growth charts of the patient
- Encourage the patient for frequent small meals to maximize calorie intake
- Advise on adequate oral hydration should be considered
Neurologic assessment
- In patients with Hutchinson-Gilford progeria syndrome (HGPS) investigate for any symptoms of the following:[5]
- Transient ischemic attack(TIA)
- Stroke
- Brain and neck magnetic resonance imaging (MRI)
- Carotid duplex scans- vascular status status
Musculoskeletal assessment
Dental assessment
- In patients with Hutchinson-Gilford progeria syndrome (HGPS) for every six months routine dental evaluation is recommended.
Ophthalmologic assessment
- In patients with Hutchinson-Gilford progeria syndrome (HGPS) annual ophthalmology assessment is considered for the following:
- Exposure keratopathy
Hearing assessment
- In patients with Hutchinson-Gilford progeria syndrome (HGPS) annual hearing assessment should be considered for the following:
- Conductive hearing loss
References
References
- ↑ Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K; et al. (1993). “GeneReviews®”. PMID 20301300.
- ↑ Ackerman J, Gilbert-Barness E (2002). “Hutchinson-Gilford progeria syndrome: a pathologic study”. Pediatr Pathol Mol Med. 21 (1): 1–13. PMID 11842974.
- ↑ Doubaj Y, Lamzouri A, Elalaoui SC, Laarabi FZ, Sefiani A (2011). “[Three cases of Hutchinson-Gilford progeria syndrome]”. Arch Pediatr. 18 (2): 156–9. doi:10.1016/j.arcped.2010.11.014. PMID 21251803.
- ↑ Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M; et al. (2012). “An inherited LMNA gene mutation in atypical Progeria syndrome”. Am J Med Genet A. 158A (11): 2881–7. doi:10.1002/ajmg.a.35557. PMID 22991222.
- ↑ Doubaj Y, Lamzouri A, Elalaoui SC, Laarabi FZ, Sefiani A (2011). “[Three cases of Hutchinson-Gilford progeria syndrome]”. Arch Pediatr. 18 (2): 156–9. doi:10.1016/j.arcped.2010.11.014. PMID 21251803.
- ↑ Cleveland RH, Gordon LB, Kleinman ME, Miller DT, Gordon CM, Snyder BD; et al. (2012). “A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndrome”. Pediatr Radiol. 42 (9): 1089–98. doi:10.1007/s00247-012-2423-1. PMC 4220680. PMID 22752073.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]