Impact of 22q Deletion Syndrome on Speech Outcomes following Primary Surgery for Submucous Cleft Palate

被引:33
|
作者
Bezuhly, Michael
Fischbach, Simone
Klaiman, Paula
Fisher, David M. [1 ]
机构
[1] Univ Toronto, Cleft Lip & Palate Program, Hosp Sick Children, Div Plast & Reconstruct Surg, Toronto, ON M5G 1X8, Canada
关键词
VELOPHARYNGEAL INSUFFICIENCY; VELOCARDIOFACIAL SYNDROME; PHARYNGEAL FLAP; SURGICAL-MANAGEMENT; FURLOW PALATOPLASTY; MANIFESTATIONS; INCOMPETENCE; CHILDREN;
D O I
10.1097/PRS.0b013e3182402e52
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Patients with 22q deletion syndrome are at increased risk of submucous cleft palate and velopharyngeal insufficiency. The authors' aim is to evaluate speech outcomes following primary Furlow palatoplasty or pharyngeal flap for correction of velopharyngeal insufficiency in submucous cleft palate patients with and without 22q deletion syndrome. Methods: Records of submucous cleft palate patients who underwent primary surgery between 2001 and 2010 were reviewed. Data included 22q deletion syndrome diagnosis, age at surgery, procedure, preoperative nasopharyngoscopy and nasometry, speech outcomes, complications, and secondary surgery rates. Results: Seventy-eight submucous cleft palate patients were identified. Twenty-three patients had 22q deletion syndrome. Fewer 22q deletion syndrome patients obtained normal resonance on perceptual assessment compared with nonsyndromic patients (74 percent versus 88 percent). A similar difference existed based on postoperative nasometric scores. Among22q deletion syndrome patients, similar success rates were achieved with Furlow palatoplasty and pharyngeal flap. No difference in the proportion improved postoperatively was noted between 22q deletion syndrome and nonsyndromic groups. One complication was experienced per group. More revision operations were indicated in the 22q deletion syndrome group (17 percent) compared with the nonsyndromic group (4 percent). Median times to normal resonance for 22q deletion syndrome and nonsyndromic patients were 150 weeks and 34 weeks, respectively. Adjusting for multiple variables, 22q deletion syndrome patients were 3.6 times less likely to develop normal resonance. Conclusion: Careful selection of Furlow palatoplasty or pharyngeal flap for primary repair of submucous cleft palate is highly effective in 22q deletion syndrome patients and yields results approaching those of nonsyndromic patients. (Plast. Reconstr. Surg. 129: 502e, 2012.)
引用
收藏
页码:502E / 510E
页数:9
相关论文
共 50 条
  • [41] Effects of a functional COMT polymorphism on neurocognitive function in the 22q deletion syndrome
    Bearden, CE
    Simon, TJ
    Wang, PP
    Jawad, AF
    Lynch, DR
    Emanuel, BS
    BIOLOGICAL PSYCHIATRY, 2003, 53 (08) : 169S - 169S
  • [42] Clozapine-associated seizures in a 22q deletion syndrome subtype of schizophrenia
    Caluseriu, O
    Tayyeb, T
    Chow, E
    Bassett, AS
    SCHIZOPHRENIA RESEARCH, 2003, 60 (01) : 79 - 79
  • [43] Stephanie's story: Caring for a child with Terminal 22q Deletion Syndrome
    Axel, SM
    Wermuth, KG
    PEDIATRICS, 2005, 115 (02) : 512 - 512
  • [44] A Comparative Study Evaluating Speech Outcomes in Classic versus Occult Submucous Cleft Palate Using a Primary Furlow Palatoplasty Technique
    Denadai, Rafael
    Chou, Pang-Yun
    Bergonzani, Michela
    Sato, Nobuhiro
    Yun, Claudia
    Lo, Lun-Jou
    PLASTIC AND RECONSTRUCTIVE SURGERY, 2020, 146 (03) : 589 - 598
  • [45] Supporting children with genetic syndromes in the classroom: the example of 22q deletion syndrome
    Reilly, Colin
    Stedman, Lindsey
    SUPPORT FOR LEARNING, 2013, 28 (03) : 115 - 121
  • [46] 18q22.3 → 18q23 Deletion Syndrome and Cleft Palate
    Eudy, James D.
    Pickering, Diane L.
    Lutz, Richard
    Platt, Kristal
    Dave, Bhavana J.
    Olney, Ann Haskins
    Sanger, Warren G.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (04) : 1046 - 1048
  • [47] TOO NEAR, YET TOO FAR: 22Q DELETION AND VELOCARDIOFACIAL SYNDROME MIMIC
    Kerber, A.
    Joshi, A.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2022, 129 : S134 - S134
  • [48] Current Practice in Assessing and Reporting Speech Outcomes of Cleft Palate and Velopharyngeal Surgery: A Survey of Cleft Palate/Craniofacial Professionals
    Kummer, Ann W.
    Clark, Stacey L.
    Redle, Erin E.
    Thomsen, Leisa L.
    Billmire, David A.
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 2012, 49 (02): : 146 - 152
  • [49] Cleft Palate in a Patient with the Nested 22q11.2 LCR C to D Deletion
    Williams, Crescenda L.
    Nelson, Katherine R.
    Grant, John H.
    Mikhail, Fady M.
    Robin, Nathaniel H.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (01) : 260 - 262
  • [50] Two sisters with different chromosomal microdeletions: Rubinstein-Taybi syndrome and 22q deletion syndrome
    Can, B
    Qu, Y
    Jackson, LG
    Floyd, M
    Say, B
    CLINICAL GENETICS, 1998, 54 (04) : 371 - 372