Zorgstandaard Marshall-Smith Syndroom

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[12] J. P. Johnson, J. C. Carey, F. J. Glassy, T. Paglieroni, and M.
H. Lipson, “Marshall-Smith syndrome: two case reports and
a review of pulmonary manifestations,” Pediatrics, vol. 71,
no. 2, pp. 219–23, 1983.
[13] D. Sperli, D. Concolino, C. Barbato, P. Strisciuglio, and G.
Andria, “Long survival of a patient with Marshall-Smith syn-
drome without respiratory complications,” J. Med. Genet.,
vol. 30, no. 10, pp. 877–9, 1993.
[14] L. van den Engel-Hoek, C. E. Erasmus, J. C. M. Hen-
driks, A. C. H. Geurts, W. M. Klein, S. Pillen, L. T. Sie, B.
J. M. de Swart, and I. J. M. de Groot, “Oral muscles are
progressivelyaffected in Duchenne muscular dystrophy:
implications for dysphagia treatment,” J. Neurol. , vol. 260,
no. 5, pp. 1295–1303, May 2013.
[15] A. Charon, Y. Gillerot, L. Van Maldergem, M. H. Van Schaf-
tingen, B. de Bont, and L. Koulischer, “The Marshall-Smith
syndrome,” Eur. J. Pediatr., vol. 150, no. 1, pp. 54–5, 1990.
[16] M. Diab, M. Raff, and D. F. Gunther, “Osseous fragility in
Marshall-Smith syndrome,” Am. J. Med. Genet., vol. 119A,
no. 2, pp. 218–22, 2003.
[17] M. Hassan, T. Sutton, K. Mage, J. M. Limal, and R. Rappa-
port, “The syndrome of accelerated bone maturation in the
newborn infant with dysmorphism and congenital malfor-
mations. (The so-called Marshall-Smith syndrome),” Pediatr.
Radiol., vol. 5, no. 1, pp. 53–7, 1976.
[18] D. Timmers-Huigens, Ervaringsordening. Reed Business,
2005.
[19] T. Koeleman, Ervaar het maar’. Een methodische werkwijze
voor stimulering van motoriek, zintuigen en communica-
tie in de begeleiding van mensen met een ernstig meer­
voudige handicap. Zutphen, 2001.
[20] I. D. C. van Balkom, A. Shaw, P. J. Vuijk, M. Franssens, H. W.
Hoek, and R. C. M. Hennekam, “Development and beha-
viour in Marshall-Smith syndrome: an exploratory study of
cognition, phenotype and autism,” J. Intellect. Disabil. Res.
JIDR, vol. 55, no. 10, pp. 973–987, Oct. 2011.
[21] M. Zenker, “submitted.”
[22] R. C. Hennekam, “Care for patients with ultra-rare disor-
ders,” Eur. J. Med. Genet., vol. 54, no. 3, pp. 220–4, 2011.
[23] M. B. Bronner, H. Knoester, A. P. Bos, B. F. Last, and M. A.
Grootenhuis, “Follow-up after paediatric intensive care tre-
atment: parental posttraumatic stress,” Acta Paediatr. Oslo
Nor. 1992, vol. 97, no. 2, pp. 181–186, Feb. 2008.
[24] B. L. da S. Mandim, N. M. Fonseca, R. A. Ruzi, and P. C.
S. Temer, “[Anesthesia in a patient with Marshall-Smith
syndrome: case report],” Rev. Bras. Anestesiol., vol. 57, no.
4, pp. 401–405, Aug. 2007.
[25] A. Cullen, T. A. Clarke, and T. P. O’Dwyer, “The Mars-
hall-Smith syndrome: a review of the laryngeal complicati-
ons,” Eur. J. Pediatr., vol. 156, no. 6, pp. 463–4, 1997.
[26] H. Antila, T. Laitio, R. Aantaa, P. Silvoniemi, and A. Pak-
kanen, “Difficult airway in a patient with Marshall-Smith
syndrome,” Paediatr. Anaesth., vol. 8, no. 5, pp. 429–432,
1998.