draditithegreat
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Library: Orthopaedics: Ellis-van Creveld Syndrome
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06.29.05 (3 years ago)
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CASE HISTORY:
A 6-month old Amish infant female was referred for symmetric polydactyly of both hands. Prior to her presentation in clinic she was seen and evaluated by a cardiologist for an apparent congenital heart murmur. There is no history of duplicate digits in either parent, however, there is a positive family history of the Ellis-van Creveld Syndrome in a third cousin.
PHYSICAL EXAM:
On physical examination of the upper extremities there was a sixth digit on the ulnar border of both hands. The finger nails appeared to be dysplastic. The remaining physical exam revealed a midline cleft in the upper lip. The upper and lower extremities were shortened out of proportion to the trunk, and the shortening in the lower extremities isolated to the tibial segments.
RADIOGRAPHS:
Plain x-ray's showed a sixth metacarpal and phalanx on the ulnar border of both hands . The distal phalanges are shortened relative to the proximal and distal segments. The pelvis has small, squared iliac crests with spikes of bone at the triradiate cartilages. The tibial segments are disproportionately shorter than the femoral segments.
DISCUSSION:
Epidemiology
Chondroectodermal dysplasia, also known as the Ellis-van Creveld Syndrome, is an autosomal recessive skeletal dysplasia that results in short-limbed disproportionate dwarfism. The disorder was first described in 1940 by Ellis and van Creveld . The term chondroectodermal is used to describe the types of tissues involved in the disorder, mainly that involvement of the long bones of the skeleton, nails and teeth. The term mesoectodermal dysplasia was once proposed to include the 60% incidence of congenital heart disease that occurs in association with the disorder.
The Ellis-van Creveld syndrome most commonly occurs in the Amish of Lancaster, Pa. but is not isolated to this group, with the incidence being approximately 5 or more per 1000 live births and 2 per 1000 living persons. The disorder has also been described in English, Dutch, Jewish, Turkish, French-Canadian and a few other persons. No case had been described in the Amish of Ohio, Indiana, or other Amish areas at the time of an extensive search performed by McKusick, et al.
The genealogy of the disorder in the Amish of Lancaster, Pa. can be traced back to the immigrants Samuel King and his wife.
Clinical Features
Post-axial polydactyly in the hands, i.e. an extra finger lateral to the normal fifth finger, is a consistent finding. Polydactyly in the feet is a rare finding.
The bone dysplasia is characterized by acromesomelia, i.e. relative shortening of the distal (acromelic) and middle (mesomelic) segments, as opposed to the proximal (rhizomelic) segments. This is especially demonstrated in the hand, where the distal and middle phalangeal segments are proportionately shorter than the proximal segments, which may interfere with the ability to make a tight fist.
There may be a valgus deformity of the knees that develops, frequently progressing and causing a significant malalignment.
The nails of the fingers and toes are dysplastic
The lip deformity, often referred to as a "partial hairlip", results from an abnormally short upper lip which may also be sunken secondary to hypoplasia of the maxilla.
The teeth are affected, with eruption occurring at birth or shortly thereafter.
Congenital heart defects may include hypoplasia of the aorta, atrial and ventricular septal defects, and a single atrium
Radiographic Features
As mentioned previously, the shorter distal and middle phalangeal segments in relation to the proximal phalangeal segments.
Multiple variations of carpal fusions, with the most common between the hamate and a ninth carpal bone.
Characteristic features of the pelvis includes:
small iliac crests and sciatic notches
originating from the triradiate cartilage a distally directed spike of bone
The proximal tibial epiphysis has a growth failure which results in a valgus deformity of the knee
The fibula is disproportionately shorter than the tibia
Treatment of orthopaedic problems
Polydactyly (surgical treatment usually between 6 mo.-1 yr.)
type I -- extra soft tissue mass not adherent to skeleton and devoid of bone, cartilage, joint or tendon: usually can be treated in the nursery by tying off the base
type II -- digits may show duplication with normal components, e.g. bifid metacarpal: treatment usually more complicated, with removal of extra tissue and correction of the deviated digit
type III -- complete digit with its own metacarpal and all soft tissues: excision of the digit and usually the metacarpal to narrow the hand
Genu valgum
if deformity is greater than 15-20 degrees, realignment osteotomy is indicated
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