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Volumn 31, Issue 8, 2015, Pages 711-717

Hirschsprung’s disease in children with Mowat–Wilson syndrome

Author keywords

Aganglionosis; Enteric neural crest; Hirschsprung; Mowat Wilson; ZEB2

Indexed keywords

AGANGLIONOSIS; ANORECTAL MALFORMATION; ARTICLE; CHILD; CLINICAL FEATURE; CLINICAL STUDY; COLOSTOMY; CRYPTORCHISM; FEMALE; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HIRSCHSPRUNG DISEASE; HUMAN; HYDRONEPHROSIS; HYPOSPADIAS; ILEOSTOMY; INTESTINE FUNCTION; MALE; PATENT DUCTUS ARTERIOSUS; PREVALENCE; PRIORITY JOURNAL; PULL THROUGH OPERATION; PYLORUS STENOSIS; RISK FACTOR; SYSTEMATIC REVIEW; TREATMENT OUTCOME; UROGENITAL TRACT MALFORMATION; VESICOURETERAL REFLUX; WILSON DISEASE; COMPLICATION; FACIES; INTELLECTUAL DISABILITY; MICROCEPHALY;

EID: 84938419568     PISSN: 01790358     EISSN: 14379813     Source Type: Journal    
DOI: 10.1007/s00383-015-3732-x     Document Type: Article
Times cited : (30)

References (60)
  • 2
    • 0031853185 scopus 로고    scopus 로고
    • Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23
    • COI: 1:STN:280:DyaK1czotlyluw%3D%3D, PID: 9719364
    • Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Ades LC, Chia NL, Wilson MJ (1998) Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J Med Genet 35(8):617–623
    • (1998) J Med Genet , vol.35 , Issue.8 , pp. 617-623
    • Mowat, D.R.1    Croaker, G.D.2    Cass, D.T.3    Kerr, B.A.4    Chaitow, J.5    Ades, L.C.6    Chia, N.L.7    Wilson, M.J.8
  • 4
    • 77953933416 scopus 로고    scopus 로고
    • Hirschsprung’s disease
    • PID: 20610192
    • Kenny SE, Tam PK, Garcia-Barcelo M (2010) Hirschsprung’s disease. Semin Pediatr Surg 19(3):194–200. doi:10.1053/j.sempedsurg.2010.03.004
    • (2010) Semin Pediatr Surg , vol.19 , Issue.3 , pp. 194-200
    • Kenny, S.E.1    Tam, P.K.2    Garcia-Barcelo, M.3
  • 5
    • 84883457883 scopus 로고    scopus 로고
    • Hirschsprung’s disease associated with Down syndrome: a meta-analysis of incidence, functional outcomes and mortality
    • PID: 23943251
    • Friedmacher F, Puri P (2013) Hirschsprung’s disease associated with Down syndrome: a meta-analysis of incidence, functional outcomes and mortality. Pediatr Surg Int 29(9):937–946. doi:10.1007/s00383-013-3361-1
    • (2013) Pediatr Surg Int , vol.29 , Issue.9 , pp. 937-946
    • Friedmacher, F.1    Puri, P.2
  • 6
    • 84871456004 scopus 로고    scopus 로고
    • Chromosomal and related Mendelian syndromes associated with Hirschsprung’s disease
    • COI: 1:STN:280:DC%2BC38bpt1eguw%3D%3D, PID: 23001136
    • Moore SW (2012) Chromosomal and related Mendelian syndromes associated with Hirschsprung’s disease. Pediatr Surg Int 28(11):1045–1058. doi:10.1007/s00383-012-3175-6
    • (2012) Pediatr Surg Int , vol.28 , Issue.11 , pp. 1045-1058
    • Moore, S.W.1
  • 7
    • 84908355989 scopus 로고    scopus 로고
    • The association between Hirschsprung’s disease and multiple endocrine neoplasia type 2a: a systematic review
    • PID: 24972642
    • Coyle D, Friedmacher F, Puri P (2014) The association between Hirschsprung’s disease and multiple endocrine neoplasia type 2a: a systematic review. Pediatr Surg Int 30(8):751–756. doi:10.1007/s00383-014-3538-2
    • (2014) Pediatr Surg Int , vol.30 , Issue.8 , pp. 751-756
    • Coyle, D.1    Friedmacher, F.2    Puri, P.3
  • 8
    • 79960626987 scopus 로고    scopus 로고
    • Clinical utility gene card for: Mowat–Wilson/syndrome
    • Zollino M, Garavelli L, Rauch A (2011) Clinical utility gene card for: Mowat–Wilson/syndrome. Eur J Hum Genet 19(8). doi:10.1038/ejhg.2011.12
    • (2011) Eur J Hum Genet , vol.19 , Issue.8
    • Zollino, M.1    Garavelli, L.2    Rauch, A.3
  • 11
    • 24344509187 scopus 로고    scopus 로고
    • Variations in aganglionic segment length of the enteric neural plexus in Mowat–Wilson syndrome
    • PID: 16150342
    • Ishihara N, Shimada A, Kato J, Niimi N, Tanaka S, Miura K, Suzuki T, Wakamatsu N, Nagaya M (2005) Variations in aganglionic segment length of the enteric neural plexus in Mowat–Wilson syndrome. J Pediatr Surg 40(9):1411–1419. doi:10.1016/j.jpedsurg.2005.05.040
    • (2005) J Pediatr Surg , vol.40 , Issue.9 , pp. 1411-1419
    • Ishihara, N.1    Shimada, A.2    Kato, J.3    Niimi, N.4    Tanaka, S.5    Miura, K.6    Suzuki, T.7    Wakamatsu, N.8    Nagaya, M.9
  • 14
    • 84900794352 scopus 로고    scopus 로고
    • Hirschsprung’s disease associated with Mowat–Wilson syndrome
    • Patel RV, Elmalik K, Bouhadiba N, Shawis R (2014) Hirschsprung’s disease associated with Mowat–Wilson syndrome. BMJ Case Rep. doi:10.1136/bcr-2013-203262
    • (2014) BMJ Case Rep
    • Patel, R.V.1    Elmalik, K.2    Bouhadiba, N.3    Shawis, R.4
  • 16
    • 84921785422 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome: neurological and molecular study in seven patients
    • PID: 25608121
    • Paz JA, Kim CA, Goossens M, Giurgea I, Marques-Dias MJ (2015) Mowat-Wilson syndrome: neurological and molecular study in seven patients. Arq Neuropsiquiatr 73(1):12–17. doi:10.1590/0004-282X20140182
    • (2015) Arq Neuropsiquiatr , vol.73 , Issue.1 , pp. 12-17
    • Paz, J.A.1    Kim, C.A.2    Goossens, M.3    Giurgea, I.4    Marques-Dias, M.J.5
  • 19
    • 84927626933 scopus 로고    scopus 로고
    • ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome
    • PID: 25028418
    • Buraniqi E, Moodley M (2015) ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome. J Child Neurol 30(1):32–36. doi:10.1177/0883073814535501
    • (2015) J Child Neurol , vol.30 , Issue.1 , pp. 32-36
    • Buraniqi, E.1    Moodley, M.2
  • 20
    • 84927712953 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome: deafness in the first Egyptian case who was conceived by intracytoplasmic sperm injection
    • 29(12):NP168–NP170 10.1177/0883073813509120
    • Abdalla EM, Zayed LH (2014) Mowat-Wilson syndrome: deafness in the first Egyptian case who was conceived by intracytoplasmic sperm injection. J Child Neurol 29(12):NP168–NP170. doi:10.1177/0883073813509120
    • (2014) J Child Neurol
    • Abdalla, E.M.1    Zayed, L.H.2
  • 21
    • 84890551994 scopus 로고    scopus 로고
    • Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association
    • PID: 24263623
    • Tanteles GA, Christophidou-Anastasiadou V (2014) Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association. Clin Dysmorphol 23(1):20–23. doi:10.1097/MCD.0000000000000013
    • (2014) Clin Dysmorphol , vol.23 , Issue.1 , pp. 20-23
    • Tanteles, G.A.1    Christophidou-Anastasiadou, V.2
  • 23
    • 84886747808 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome detected by using high resolution microarray
    • COI: 1:CAS:528:DC%2BC3sXhsFOhsrvI, PID: 24029077
    • Park JY, Cho EH, Lee EH, Kang YS, Jun KR, Hur YJ (2013) Mowat-Wilson syndrome detected by using high resolution microarray. Gene 532(2):307–309. doi:10.1016/j.gene.2013.07.067
    • (2013) Gene , vol.532 , Issue.2 , pp. 307-309
    • Park, J.Y.1    Cho, E.H.2    Lee, E.H.3    Kang, Y.S.4    Jun, K.R.5    Hur, Y.J.6
  • 25
    • 84873197186 scopus 로고    scopus 로고
    • A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene
    • PID: 23427518
    • Meral C, Malbora B, Celikel F, Aydemir G, Suleymanoglu S, Zollino M, Derbent M (2012) A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene. Turk J Pediatr 54(5):523–527
    • (2012) Turk J Pediatr , vol.54 , Issue.5 , pp. 523-527
    • Meral, C.1    Malbora, B.2    Celikel, F.3    Aydemir, G.4    Suleymanoglu, S.5    Zollino, M.6    Derbent, M.7
  • 27
    • 84864223139 scopus 로고    scopus 로고
    • Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2
    • COI: 1:CAS:528:DC%2BC38XhtFSqtb7F, PID: 22486326
    • Ariss M, Natan K, Friedman N, Traboulsi EI (2012) Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2. Ophthalmic Genet 33(3):159–160. doi:10.3109/13816810.2011.610860
    • (2012) Ophthalmic Genet , vol.33 , Issue.3 , pp. 159-160
    • Ariss, M.1    Natan, K.2    Friedman, N.3    Traboulsi, E.I.4
  • 28
    • 79954626489 scopus 로고    scopus 로고
    • Avoiding pitfalls in molecular genetic testing: case studies of high-resolution array comparative genomic hybridization testing in the definitive diagnosis of Mowat-Wilson syndrome
    • COI: 1:CAS:528:DC%2BC3MXntlyis7w%3D, PID: 21497296
    • Kluk MJ, An Y, James P, Coulter D, Harris D, Wu BL, Shen Y (2011) Avoiding pitfalls in molecular genetic testing: case studies of high-resolution array comparative genomic hybridization testing in the definitive diagnosis of Mowat-Wilson syndrome. J Mol Diagn 13(3):363–367. doi:10.1016/j.jmoldx.2011.01.008
    • (2011) J Mol Diagn , vol.13 , Issue.3 , pp. 363-367
    • Kluk, M.J.1    An, Y.2    James, P.3    Coulter, D.4    Harris, D.5    Wu, B.L.6    Shen, Y.7
  • 29
    • 79952315393 scopus 로고    scopus 로고
    • Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development
    • PID: 21336163
    • Cui S, Erlichman J, Russo P, Haber BA, Matthews RP (2011) Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development. J Pediatr Gastroenterol Nutr 52(3):339–344. doi:10.1097/MPG.0b013e3181ff2e5b
    • (2011) J Pediatr Gastroenterol Nutr , vol.52 , Issue.3 , pp. 339-344
    • Cui, S.1    Erlichman, J.2    Russo, P.3    Haber, B.A.4    Matthews, R.P.5
  • 30
    • 77951916275 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome: the first two Malaysian cases
    • COI: 1:STN:280:DC%2BC3c3pslCjug%3D%3D, PID: 20428734
    • Balasubramaniam S, Keng WT, Ngu LH, Michel LG, Irina G (2010) Mowat-Wilson syndrome: the first two Malaysian cases. Singapore Med J 51(3):e54–57
    • (2010) Singapore Med J , vol.51 , Issue.3 , pp. e54-e57
    • Balasubramaniam, S.1    Keng, W.T.2    Ngu, L.H.3    Michel, L.G.4    Irina, G.5
  • 31
    • 79952278408 scopus 로고    scopus 로고
    • Supernumerary intestinal muscle coat in a patient with Hirschsprung disease/Mowat-Wilson syndrome
    • PID: 20158378
    • Leong M, Verey F, Newbury-Ecob R, Ramani P (2010) Supernumerary intestinal muscle coat in a patient with Hirschsprung disease/Mowat-Wilson syndrome. Pediatric and developmental pathology 13(5):415–418. doi:10.2350/09-09-0715-CR.1
    • (2010) Pediatr Dev Pathol , vol.13 , Issue.5 , pp. 415-418
    • Leong, M.1    Verey, F.2    Newbury-Ecob, R.3    Ramani, P.4
  • 32
    • 76649113394 scopus 로고    scopus 로고
    • Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient
    • COI: 1:STN:280:DC%2BC3c7gt1ektg%3D%3D, PID: 20145308
    • Smigiel R, Szafranska A, Czyzewska M, Rauch A, Zweier C, Patkowski D (2010) Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient. J Appl Genet 51(1):111–113
    • (2010) J Appl Genet , vol.51 , Issue.1 , pp. 111-113
    • Smigiel, R.1    Szafranska, A.2    Czyzewska, M.3    Rauch, A.4    Zweier, C.5    Patkowski, D.6
  • 33
    • 75449117085 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome with associated dysphagia
    • PID: 20101699
    • Prijoles EJ, Adam M (2010) Mowat-Wilson syndrome with associated dysphagia. Am J Med Genet A 152A(2):484–485. doi:10.1002/ajmg.a.33211
    • (2010) Am J Med Genet A , vol.152A , Issue.2 , pp. 484-485
    • Prijoles, E.J.1    Adam, M.2
  • 35
    • 58849102581 scopus 로고    scopus 로고
    • Safe use of the classic laryngeal mask airway and endotracheal intubation in general anaesthesia for a patient with Mowat-Wilson syndrome
    • PID: 19207908
    • Kiernan F, Crowe S (2009) Safe use of the classic laryngeal mask airway and endotracheal intubation in general anaesthesia for a patient with Mowat-Wilson syndrome. Paediatr Anaesth 19(2):174–175. doi:10.1111/j.1460-9592.2008.02888.x
    • (2009) Paediatr Anaesth , vol.19 , Issue.2 , pp. 174-175
    • Kiernan, F.1    Crowe, S.2
  • 38
    • 42449087624 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p. T791fsX816)
    • PID: 18259761
    • Sasso A, Paucic-Kirincic E, Kamber-Makek S, Sindicic N, Brajnovic-Zaputovic S, Brajenovic-Milic B (2008) Mowat-Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p. T791fsX816). Childs Nerv Syst 24(5):615–618. doi:10.1007/s00381-007-0557-5
    • (2008) Childs Nerv Syst , vol.24 , Issue.5 , pp. 615-618
    • Sasso, A.1    Paucic-Kirincic, E.2    Kamber-Makek, S.3    Sindicic, N.4    Brajnovic-Zaputovic, S.5    Brajenovic-Milic, B.6
  • 40
    • 37849004083 scopus 로고    scopus 로고
    • Mowat-Wilson syndrome with craniosynostosis: a case report
    • PID: 18076118
    • Adam MP, Justice AN, Bean LJ, Fernhoff PM (2008) Mowat-Wilson syndrome with craniosynostosis: a case report. Am J Med Genet A 146A(2):245–246. doi:10.1002/ajmg.a.32075
    • (2008) Am J Med Genet A , vol.146A , Issue.2 , pp. 245-246
    • Adam, M.P.1    Justice, A.N.2    Bean, L.J.3    Fernhoff, P.M.4
  • 41
    • 84946396869 scopus 로고    scopus 로고
    • Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome
    • COI: 1:CAS:528:DC%2BD2sXhtleqtLnM, PID: 17932455
    • Sasongko TH, Sadewa AH, Gunadi, Lee MJ, Koterazawa K, Nishio H (2007) Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome. Kobe J Med Sci 53(4):157–162
    • (2007) Kobe J Med Sci , vol.53 , Issue.4 , pp. 157-162
    • Sasongko, T.H.1    Sadewa, A.H.2    Gunadi, L.M.J.3    Koterazawa, K.4    Nishio, H.5
  • 43
    • 34447304048 scopus 로고    scopus 로고
    • Pulmonary artery sling and congenital tracheal stenosis in another patient with Mowat-Wilson syndrome
    • COI: 1:CAS:528:DC%2BD2sXosVygsLY%3D, PID: 17567886
    • Strenge S, Heinritz W, Zweier C, Rauch A, Rolle U, Merkenschlager A, Froster UG (2007) Pulmonary artery sling and congenital tracheal stenosis in another patient with Mowat-Wilson syndrome. Am J Med Genet A 143A(13):1528–1530. doi:10.1002/ajmg.a.31801
    • (2007) Am J Med Genet A , vol.143A , Issue.13 , pp. 1528-1530
    • Strenge, S.1    Heinritz, W.2    Zweier, C.3    Rauch, A.4    Rolle, U.5    Merkenschlager, A.6    Froster, U.G.7
  • 44
    • 33947189049 scopus 로고    scopus 로고
    • A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features
    • COI: 1:STN:280:DC%2BD2s7msFyisQ%3D%3D, PID: 17223398
    • Hoffer MJ, Hilhorst-Hofstee Y, Knijnenburg J, Hansson KB, Engelberts AC, Laan LA, Bakker E, Rosenberg C (2007) A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features. Eur J Med Genet 50(2):149–154. doi:10.1016/j.ejmg.2006.11.004
    • (2007) Eur J Med Genet , vol.50 , Issue.2 , pp. 149-154
    • Hoffer, M.J.1    Hilhorst-Hofstee, Y.2    Knijnenburg, J.3    Hansson, K.B.4    Engelberts, A.C.5    Laan, L.A.6    Bakker, E.7    Rosenberg, C.8
  • 45
    • 33744828021 scopus 로고    scopus 로고
    • A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype
    • PID: 16688751
    • Heinritz W, Zweier C, Froster UG, Strenge S, Kujat A, Syrbe S, Rauch A, Schuster V (2006) A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype. Am J Med Genet A 140(11):1223–1227. doi:10.1002/ajmg.a.31267
    • (2006) Am J Med Genet A , vol.140 , Issue.11 , pp. 1223-1227
    • Heinritz, W.1    Zweier, C.2    Froster, U.G.3    Strenge, S.4    Kujat, A.5    Syrbe, S.6    Rauch, A.7    Schuster, V.8
  • 46
    • 33645568819 scopus 로고    scopus 로고
    • Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype
    • PID: 16532472
    • Zweier C, Horn D, Kraus C, Rauch A (2006) Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype. Am J Med Genet A 140(8):869–872. doi:10.1002/ajmg.a.31196
    • (2006) Am J Med Genet A , vol.140 , Issue.8 , pp. 869-872
    • Zweier, C.1    Horn, D.2    Kraus, C.3    Rauch, A.4
  • 49
    • 0346096487 scopus 로고    scopus 로고
    • Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome)
    • COI: 1:CAS:528:DC%2BD2cXht1Sju7w%3D, PID: 14681759
    • Sztriha L, Espinosa-Parrilla Y, Gururaj A, Amiel J, Lyonnet S, Gerami S, Johansen JG (2003) Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome). Neuropediatrics 34(6):322–325. doi:10.1055/s-2003-44671
    • (2003) Neuropediatrics , vol.34 , Issue.6 , pp. 322-325
    • Sztriha, L.1    Espinosa-Parrilla, Y.2    Gururaj, A.3    Amiel, J.4    Lyonnet, S.5    Gerami, S.6    Johansen, J.G.7
  • 50
    • 0942287850 scopus 로고    scopus 로고
    • Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease
    • PID: 14679597
    • Horn D, Weschke B, Zweier C, Rauch A (2004) Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease. Am J Med Genet A 124A(1):102–104. doi:10.1002/ajmg.a.20298
    • (2004) Am J Med Genet A , vol.124A , Issue.1 , pp. 102-104
    • Horn, D.1    Weschke, B.2    Zweier, C.3    Rauch, A.4
  • 52
    • 0037087243 scopus 로고    scopus 로고
    • "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene
    • PID: 11891681
    • Zweier C, Albrecht B, Mitulla B, Behrens R, Beese M, Gillessen-Kaesbach G, Rott HD, Rauch A (2002) "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene. Am J Med Genet 108(3):177–181
    • (2002) American journal of medical genetics , vol.108 , Issue.3 , pp. 177-181
    • Zweier, C.1    Albrecht, B.2    Mitulla, B.3    Behrens, R.4    Beese, M.5    Gillessen-Kaesbach, G.6    Rott, H.D.7    Rauch, A.8
  • 55
    • 84938420622 scopus 로고    scopus 로고
    • Common treatment, rare complication
    • Prajapati H. FE (2012) Common treatment, rare complication. Pediatr Nephrol 27(9):1664
    • (2012) Pediatric Nephrology , vol.27 , Issue.9 , pp. 1664
    • Prajapati, H.F.E.1
  • 59
    • 84938414966 scopus 로고    scopus 로고
    • Novel dermatological manifestations of Mowat-Wilson syndrome including photosensitivity and dyspigmentation
    • Kaur B, Taibjee, S., Abdullah, A., Shannon, N. (2010) Novel dermatological manifestations of Mowat-Wilson syndrome including photosensitivity and dyspigmentation. Arch Disease Childhood 95(S1):A15–A16
    • (2010) Archives of Disease in Childhood , vol.95 , Issue.S1 , pp. A15-A16
    • Kaur, B.1    Taibjee, S.2    Abdullah, A.3    Shannon, N.4


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