Frequency of Surgical Correction for Maxillary Hypoplasia
in Cleft Lip and Palate
Snehlata Oberoi, DDS,* William Y. Hoffman, DDS,Þ Radhika Chigurupati, DMD,þ
and Karin Vargervik, DDS§
Objective: The aim of this study was to determine the frequen-
cy of surgical correction of maxillary hypoplasia in individuals
with nonsyndromic cleft lip and/or palate (CL/P) treated at the
Center for Craniofacial Anomalies at University of California,
San Francisco (UCSF).
Subjects: This is a retrospective cohort study of individuals with
cleft lip and/or palate born between 1970 and 1990 who were treated
at the UCSF Center for Craniofacial Anomalies. Data were gathered
from the UCSF Craniofacial Anomalies Filemaker Pro database.
Methods: From the database, we collected the following infor-
mation: age, gender, cleft type, date of orthognathic surgery, and
type of osteotomy. The subjects were further subcategorized by cleft
type and gender.
Results: A total of 973 individuals with a diagnosis of cleft lip and/or
palate were reviewed: 325 subjects had an associated syndrome and
648 were nonsyndromic. A total of 59 of these 648 nonsyndromic cleft
individuals (9.1%) required surgical intervention for correction of
maxillary hypoplasia: 2/105 (1.9%) for cleft lip, 4/122 (3.3%) for cleft
palate, 35/286 (12.2%) for unilateral cleft lip and palate, and 18/135
(13.3%) for bilateral cleft lip and palate.
Conclusions: The frequency of surgical correction for maxillary
hypoplasia in cleft individuals at UCSF Center for Craniofacial
Anomalies at 9% was lower than the reported average of 25%.
Key Words: Cleft lip/palate, maxillary hypoplasia, Le Fort
(J Craniofac Surg 2012;23: 1665Y1667)
C
left lip and/or cleft palate constitute the most common con-
genital malformation of the head and neck.
1
Many individuals
with a cleft develop maxillary hypoplasia, which includes features
such as concave facial profile, lack of adequate upper lip support
and nasal tip projection, decreased upper incisor display, and an-
terior and posterior crossbites.
2
Clinical studies of maxillary growth associated with a cleft have
yielded conflicting results. This may be due to study limitations such as
small sample size, large age range, different clinical management
protocols, failure to separate cleft types, combining of sexes, inade-
quate controls, and insufficient postoperative interval. Some
3Y5
claim
that maxillary deficiency in cleft individuals is an intrinsic primary
defect. Others
6Y8
maintain that the maxillary deficiency is primarily a
result of surgical repair.
Some investigators have tried to determine whether it is lip or
palate repair that causes deficient maxillary growth. Capelozza et al
8
found maxillary retrusion after lip repair only and those who had both
lip and palate repair did not differ significantly from the lip repair-only
group. Other authors have stated that it is the repair of the palate that
most interferes with normal maxillary growth.
7,9Y11
Maxillary growths in unilateral cleft lip and palate have been
studied in various age groups. In children younger than 8 years,
findings vary from predominantly normal
12Y14
to smaller than normal
maxillae.
15Y16
However, most studies have found smaller than normal
anterior-posterior dimensions, indicating maxillary hypoplasia in
individuals older than 11 years.
17Y21
One study reported no difference
from normal.
22
However, it is generally agreed that maxillary growth
is often diminished in individuals with repaired cleft lip and/or palate
and that this is due to a combination of intrinsic skeletal, dental, and
soft tissue deficiencies and the subsequent effects of surgical and
other interventions. The maxillary deficiency is in vertical, anterior-
posterior, and transverse dimensions, and its severity varies due to
many factors such as cleft type, timing, and type of interventions and of
interceptive treatment. When the degree of maxillary hypoplasia is
severe, surgical correction with facial osteotomies is necessary. Typi-
cally, a Le Fort I maxillary procedure is used to correct this deformity in
adolescence, after growth completion. The literature indicates that the
need for surgical correction ranges between 14% and 45% with an
average of 25%.
The aim of this study is to determine the frequency of maxillary
hypoplasia requiring surgical correction in individuals with non-
syndromic cleft lip and/or palate (CL/P) treated at the UCSF Center for
Craniofacial Anomalies.
METHODS
This retrospective cohort study was conducted on individuals
with nonsyndromic cleft lip and/or palate that had completed
growth; born between 1970 and 1990. Data were gathered from the
UCSF Craniofacial Anomalies Filemaker Pro 10.0 database (Santa
Clara, CA). Key words used were cleft lip (CL), cleft palate (CP),
cleft lip and palate (CLP), unilateral cleft lip (UCL), bilateral cleft
lip (BCL), unilateral cleft lip and palate (UCLP), and bilateral cleft
ORIGINAL ARTICLE
The Journal of Craniofacial Surgery & Volume 23, Number 6, November 2012 1665
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From the *Center for Craniofacial Anomalies, School of Dentistry, the
†Department of Surgery, School of Medicine, University of California at
San Francisco, the ‡Department of Oral and Maxillofacial Surgery,
University of Maryland, Baltimore, and the §Department of Orofacial
Sciences, School of Dentistry, University of California at San Francisco.
Received May 31, 2012.
Accepted for publication June 15, 2012.
Address correspondence and reprint requests to Snehlata Oberoi, DDS,
Division of Craniofacial Anomalies, Department of Orofacial Sciences,
School of Dentistry, University of California at San Francisco, San Francisco,
CA 94143-044; E-mail: sneha.oberoi@ucsf.edu
The authors report no conflicts of interest.
Copyright * 2012 by Mutaz B. Habal, MD
ISSN: 1049-2275
DOI: 10.1097/SCS.0b013e31826542ff
Copyright © 2012 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.