Top

Gepubliceerd in:

2014 | OriginalPaper | Hoofdstuk

Beschrijving van speciale diagnostische categorieën

augustus 2001

Auteurs : H.F.M. Peters, R. Bastiaanse, J. Van Borsel, K. Jansonius-Schultheiss, Sj. Van der Meulen, B.J.E. Mondelaers

Gepubliceerd in: Stoornissen in pimaire mondfuncties

Uitgeverij: Bohn Stafleu van Loghum

Samenvatting

In de literatuur worden vaak modellen beschreven om voedings– en slikproblemen bij kinderen adequaat te beoordelen, ook met het oog op de behandeling.

vorige hoofdstuk Voedingsproblematiek bij baby’s en jonge kinderen

volgende hoofdstuk Temporomandibulaire disfunctie en logopedie: inleiding en diagnostiek

Arvedson J.C., & Brodsky, L. (1993). Pediatric swallowing and feeding: assesment and management (p. 1 ). 1ste dr. San Diego: Singular Publishing Group, Inc.

Arvedson, J.C., & Brodsky, L. (1993). Pediatric swallowing and feeding: assesment and management(p. 77–80). 1ste dr. San Diego: Singular Publishing Group, Inc.

Arvystas, M., & Shprintzen, R.J. (1991). Craniofacial morphology in Treacher Collins Syndrome. Cleft Palate–Craniofacial Journal, 28(2), 226–231.CrossRef

Bancalari, E., & Gelhardt, T. (1986). Bronchopulmonary dysplasia. Pediatric Clinics of North America, 33, 1–23.CrossRef

Bershof, J.F., Guyuron, B., & Olsen, M.M. (1992). G syndrome: a review of the literature and a case report. Journal of Cranio–Maxillo–Facial Surgery, 20(1), 24–27.CrossRef

Bosma, J.F., Lind, J., & Truby, H.M. (1966). Distortions of upper respiratory and swallowmotions in infants having anomalies of the upper airway. Acta Paediatrica Scandinavia, 163, 112–128.

Bosma, J.F. (1967). Human infant oral function. In C.C. Thomas (red.), Symposium on oral sensation and perception. Springfield il.

Braun–Quentin, C., Kapferer, L., & Kotzot, D. (1996). Variant of coffin–Siris Syndrome of previously undescribed syndrome. American Journal of Medical Genetics, 64, 568–572.CrossRef

Budden, S.S. (1995). Management of Rett Syndrome: A ten year experience. Neuropediatrics, 26, 75–77.CrossRef

Byerly, K.A., & Pauli, R.M. (1993). Cranial nerve abnormalities in charge association. American Journal of Medical Genetics, 45(5), 751–757.CrossRef

Cannistra, C., Barbet, J.P. , Houette, A., Marchese, J.L., & Iannetti, G. (1998). Mandibulofacial dysostosis, comparison study of a neonate with mandibulo–facial dysostosis and a normal child. Journal of Cranio–Maxillo–Facial Surgery, 26(2), 92–97.CrossRef

Chandler, K.E., Die–Smulders, C.E.M. de, Engelen, J.J.M., & Schrander, J.J.P. (1997). Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion. European Journal of Pediatrics, 156, 636–638.CrossRef

Clarren, S.K., Anderson, B., & Wolf, L.S. (1987). Feeding infants with cleft lip, cleft palate, or cleft lip and palate. Cleft palate journal, 24, 244–249.

Davenport, S.L.H. (1988). Multiple congenital anomalies: an approach to management. Pediatrician, 15, 37–44.

Day–Salvatore, D., & McLean, D. (1998). Blepharophimosis, hypoplastic radius, hypoplastic left heart, telecanthus, hydronephrosis, fused metacarpals, and ‘prehensile’ halluces: a new syndrome? American Journal of Medical Genetics, 80(4), 309–313.CrossRef

De Jong, G., Nelson, M.M. (1992). Choanal atresia in two unrelated patients with the Coffin–Siris syndrome. Clinical Genetics, 42, 320–322.CrossRef

Di Rocco, M., Gatti, R., Gandullia, P., Barabino,A., Picco, P., & Borrone, C. (1993). Report on two patients with Costello syndrome and sialuria. American Journal of Medical Genetics, 47(7), 1135–1140.CrossRef

Elliott, M., Bayly, R., Cole, T., Temple, I.K., & Maher, E.R. (1994). Clinical features and natural history of Beckwith–Wiedemann syndrome: presentation of 74 new cases (see comments). Clinical Genetics, 46(2), 168–174.

Fahmy, J., Kaminsky, C.K., & Parisi, M.T. (1998). Perlman syndrome: a case report emphasizing its similarity to and distinction from Beckwith–Wiedemann and prune–belly syndromes. Pediatric Radiology, 28(3), 179–182.CrossRef

Ferry, P.C. Neurologic sequelae of cardiac surgery in children. American Journal of diseases in childhood, 141, 309–312.CrossRef

Gau, S.F., Soong, W.T., Liu, H.M., Hou, J.W., Tsai, W.Y., Chiu, Y.N., Yeh, Y.C., Wang, P.J. & Wang, T.R. (1996). Klein–Levin Syndrome in a boy with Prader–Willi Syndrome. Sleep, 19(1), 13–17.

Grady, E. (1977). Breast–feeding the baby with a cleft of the soft palate. Clinical Pediatrics, 16, 978–981.CrossRef

Grimm, S.E. III & Thomas, G.P. (1997). charge syndrome: review of literature and report of case. Coloboma, heart disease, atresia of choanae, retarded mental development, genital hypoplasia, ear abnormalities–deafness. asdcJournal of Dentistry for Children, 64(3), 218–221,228.

Hans–Heiner, K., Majewski, F., Trampisch, H.J. e.a. (1987). Malformation pattern in children with congenital heart disease. American Journal of diseases in Childhood, 141, 789–795.

Hayashi, M., Itoh, M., Kabasawa, Y., Haashi, H., Satoh, J. & Marimatsu, Y. (1992). A neuropathological study of a case of the Prader–Willi syndrome with an interstitial deletionof the proximal long arm of chromosome 15. Brain and Development 14(1),58–62.CrossRef

Herbst, J.J. (1981). Gastroesophageal reflux. Journal of Pediatrics, 98, 859–870.CrossRef

Janik, J.S., Burrington, J.D., &Withfield, J. (1986). Congenital anomalies of the lover airway. In T.J. Balkany, N.R. Pashley (red.), Clinical pediatric otolaryngology (p. 369–405). St Louis, mo: C.V. Mosby.

Jaquez, M., Drescoll, D.A., Mengrong, L., Emanuel, B.S., Hernandez, I., Jaquez, F., Lembert, N., Ramirez, J., & Matalon, T. (1997). Unbalanced 15, 22 translocation in a patient with manifestations of DiGeorge and velo–cardio–facial syndrome. American Journal of Medical Genetics, 70, 6–70.CrossRef

Johnson, J.P., Golabi, M., Norton, M.E., Rosenblatt, R.N., Feldman, G.M., Yang, S.P., hall, B.D., Fries, M.H., & Careyn, J.C. (1998). Costello syndrome: phenotype, natural history, differeential diagnosis and possible cause. Journal of Pediatrics, 95, 450–453.

Jones, K.L. (1997). Smith's recognizable patterns of human malformation. 5de dr. Philadelphia: W.B. Saunders Company.

Kawashiro, N., Koga, k., Tsuchihashi, N., & Araki, A. (1994). Choanal atresia and congenistal pharyngeal stenosis. Acta Oto Laryngologica Supplement, 517, 27–32.CrossRef

Kliegman, R.M., Pittard, W.B., & Faranoff, A.a. (1989). Necrotizing enterocolitis in neonates fed human milk. Journal of Pediatrics, 95, 450–453.CrossRef

Koomen & Hoekstra (1994). Rondom het kind: Kinderen met een schizis (p.16–105). Boom.

Lewis, M.B., & Pashayan, H.M. (1980). Management of infants with Robin anomaly. Clinical Pediatrics, 19, 519–528.CrossRef

Lewis, M.B. & Pashayan, H.M. (1980). Mangement of infants with Robin Anomaly. Clinical Pediatrics, 19(8), 519–521, 525–528.CrossRef

Limbrock, G.J., Fischer–Brandies, H., & Avalle, C. (1991). Castillo–Morales' orofacial therapy: treatment of 67 children with Down syndrome. Developmental Medicine and Child Neurology, 33 (4), 396–303.CrossRef

Lin, K.J., & Wang, W.N., (1997). Moebius syndrome: report of case. asdcJournal of Denteistry for Children, 64(1), 64–67.

Lynch, M., & Sweatt, A. (1987). Cognital heart disease: assessment and case–finding by community health nurses. Home Healthcare Nurse, 5, 32–41.CrossRef

Macrea, M.M., & Le Boeuf, M.B. (1988). Standardized nursing care plan for the open–heart surgery neonate. Neonatal network, 7, 49–57.

Massarano, A.A., Wood, A., Tait, R.C., Stevens, R., &Super, M. (1996). Noonan syndrome: coagulation and clinical aspects. Acta Paediatrica, 85(10), 1181–1185.CrossRef

Mathew, O.P. (1988). Regulation of breathing pattern during feeding: role of suck, swallow, and nutrients. In O.P. Mathew & G. Sant'Ambrogio, Respitory function of the upper airway (p. 535–560). New York: Marcel Dekker, Inc.

Mathisen, B., Reilly S., & Skuse, D. (1992). Oral–motor dysfunction and feeding disorders of infants with Turner syndrome. Developmental Medicine and Child Neurology, 34, 141–149.CrossRef

Mayo, R., Warren, D.W., & Zajac, D.J. (1998). Intraoral pressure and velopharyngeal function. Cleft Palate–Craniofacial journal, 35(4), 299–303.CrossRef

Moss, A.H.L., Jones, K., &Pigott, R.W. (1990). Submucous cleft palate in the differential diagnosis of feeding difficulties. Archives of disease in childhood, 65, 182–184.CrossRef

Noonan, J.A. (1994). Noonan syndrome. An update and review for the primary pediatrician (see comments). Clinical Pediatrics, 33(9), 548–555.CrossRef

Orenstein, S.R., Orenstein, D.M. (1988). Gastroesophageal reflux and respiratory disease in infants and children. Journal of pediatrics, 112, 847–858.

Palmer, M.M., Heyman, M.B. (1993). Assessment and treatment of sensory–versus motorbased feeding problems in very young children. Infants and young children, 6(2), 67–73.CrossRef

Park, M.K. (1984). Pediatric cardiology for practioners. Chicago, il: Year Book Medical Publishers.

Pettett, G. (1986). Medical complications of the premature infant. Physical and occupational therapy in pediatrics, 6, 91–104.CrossRef

Philip, N., & Sigaudi, S. (1998). Costello syndrome. Journal of Medical Genetics, 35, 238–240.CrossRef

Pratesi, R., Santos, M., & Ferrari, I. (1998). Costello syndrome in two Brazilian children. Journal of Medical Genetics, 35, 54–57.CrossRef

Qazi, Q.H., Heckman, L.S., Markouizos, D., & Verma, R.S. (1990). The Coffin–Siris syndrome. Journal of Medical Genetics, 27, 333–336.CrossRef

Ratner, I., & Whitfield, J. (1983). Acquired subglottic stenosis in the very–low–birth–weight infant. American journal of diseases in childhood, 137, 40–43.CrossRef

Rego, A., Coll, M.D., Regal, M., Guitart, M., Escudero, T., & Garcia–Mayor, R.V. (1997). A case with 47,XXY,del(15)(q11, q13) karyotype associated with Prader–Willi phenotype. Hormone Research, 48, 44–46.

Rimell, F.L., Shapiro, A.M., Shoemaker, D.L., & Kenna, M.A. (1995). Head and neck manifestations of Beckwith–Wiedemann syndrome. Otolaryngology Head and Neck Surgery, 113(3), 262–265.CrossRef

Rommel N., Vantrappen, G., Swillen, A., Devriendt, K., Feenstra, L., & Fryns, J.P. (1999). Retrospective analysis offeeding and speech disorders in 50 patients with velo–cardio–facial syndrome. Genetic Counselling, 10(1), 71–78.

Rommel, N., Van Limbergen J., Vanweser, K., Zegher, F. de, Daniels, H., Hoffman, I., & Veereman–Wauters, G. (1999). Severe feeding problems in children: relationship to prenatal growth and gestational age. Gastroenterology, 116(4), G4652.

Rommel N., Deman E., Veereman–Wauters, G., Devriendt, K. (1999). Voedingsproblemen bij genetische aandoeningen: literatuuroverzicht. Tijdschrift Logopedie, 12(4), 25–31.

Rommel, N. (2000). Voedingsproblemen bij kinderen met schizis. Lezing Dag van de foniatrie, 14 april, Utrecht: Academisch Ziekenhuis Utrecht.

Saenz, R.B. (1999). Primary care of infants and young children with Down Syndrome. American Family Physician, 59(2), 381–390.

Say, B., Güçavas, M., Morgan, H., & York, C. (1993). The Costello Syndrome. American Journal of Medical Genetics, 47, 163–165.CrossRef

Schwarz, S.M., Gewitz, M.H., See, C.C. e.a. (1990). Enteral nutrition in infants with congenital heart disease and growth failure. Pediatrics, 86, 368–373.

Shah, C.P., Wong, D. (1980). Management of children with cleft lip and palate. CMA Journal, 122, 19–24.

Sharland, M., Burch, M., McKenna, W.M., & Paton, M.A. (1992). A clinical study of Noonan Syndrome. Archives of Disease in Childhood, 67, 178–183.CrossRef

Shepard, R.W., Wren, J., Evans, S. e.a. (1987). Gastroesophageal reflux in infants: clinical profile, course and outcome with active therapy in 126 cases. Clinical Pediatrics, 26, 55–60.CrossRef

Shprintzen, R.J. (1988). Pierre–Robin, micrognathie and airway obstruction: the dependency of treatment on accurate diagnosis. International Anesthesiology clinics, 26, 64–71.CrossRef

Smith, A., Wiles, C., Haan, E., McGill, J., Wallace, G., Dixon, J., Selby, R., Colley, A., Mark R. & Trent, R.J. (1996). Clinical features in 27 patients with Angelman syndrome resulting from dna deletion. Journal of Medical Genetics, 33, 107–112.CrossRef

Smith, J.J., Beck, J. ( 1985). Mechanical feeding difficulties afrer primary repair of oesphageal atresia. Acta paediatrica Scandinavia,74, 237–239.CrossRef

Spender, Q., Stein, A., Dennis, J., Reilly, S., Percy, E., & Cave, D. (1996). An exploration of feeding difficulties in children with Down syndrome. Developmental Medicine and Child Neurology, 38, 681–694.CrossRef

Stone, P., Trevenen, C.L., Mitchell, I., & Rudd, N. (1990). Congenital tracheal stenosis in Pfeiffer syndrome. Clinical Genetics, 38(2), 145–148.CrossRef

Styer, G.W., Freeh, K. (1981). Feeding infants with cleft lip and/or palate. Journal of obstetric gynecologic and neonatal nursing, 10, 329-332.CrossRef

Teebi, A., & Shaabani, I.S. (1993). Further delineation of Costello Syndrome. American Journal of Medical Genetics, 47, 166–168.CrossRef

Van den Broek, P., & Feenstra, L. (1993). Zakboek Keel–, Neus–, Oorheelkunde (p. 179). Leuven: Acco.

Vanderhoof; J.A., Hofschire, P.J., Baluff; MA. e.a. (1982.). Continuous enteral feedings: an important adjunct to the management of complex congenital hean disease. American Journal of disease in children, 136, 825–827.CrossRef

Walsh, M.C., Kliegman, R.M. (1986). Necrotizing enteroclitis: treatment based on staging criteria. Pediatric Clinics of North America, 33, 179–201.CrossRef

Weatherly–White, R.C.A., Kuehn, D.P., Mirett, P. e.a. (1987). Early repair and breast–feeding for infants with cleft lip. Plastic and reconstructive surgery, 79, 879–885.CrossRef

Wolf, L.S., Glass, R.P. (1992). Special diagnostic categories. In Feeding and swallowing disorders in infancy: assessment and management (p. 297–399). Arizona: Therapy Skill Builders.

Wolfson, M.R., Bhutani, V.K., Shaffer, T.H. e.a. (1984). Mechanics and energetics of breathing helium in infants with bronchopulmonary dysplasia. Journal of Pediatrics, 104, 752–757.CrossRef

Zampino, G., Mastroiacovo, P., Ricci, R., Marcella, Z., Segni, G., Martini–Neri, M.E., & Neri, G. (1993). Costello Syndrome: Further clinical delineation, natural history , genetic definition, and nosology. American Journal of Medical Genetics, 47, 176–183.CrossRef

Zori, R.T., Hendrickson, J., Woolven, S., Whidden, E.M., Gray, B., & Williams, C.A. (1992) Angelman Syndrome: Clinical Profile. Journal of Child Neurology, 7, 270–280.CrossRef

Titel: Beschrijving van speciale diagnostische categorieën
Auteurs: H.F.M. Peters
R. Bastiaanse
J. Van Borsel
K. Jansonius-Schultheiss
Sj. Van der Meulen
B.J.E. Mondelaers
Uitgeverij: Bohn Stafleu van Loghum
Boek: Stoornissen in pimaire mondfuncties
Print ISBN: 978-90-368-0805-7

Elektronisch ISBN: 978-90-368-0806-4

Copyright: 2014
DOI: https://doi.org/10.1007/978-90-368-0806-4_3

Bohn Stafleu van Loghum

Deel dit onderdeel of sectie (kopieer de link)

Samenvatting

Log in om toegang te krijgen