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F. Chotel, A. Peltier, R. Kohler, J. Bérard

40

Conclusion

Separation of syndromes associated with

congenitaldislocationandsyndromesassociated

with patellar aplasia or hypoplasia is artificial

and used here only for a didactic point of view.

When dealing with these pathology, careful

attention must be paid during clinical exam in

order to detect associated syndromes that could

impact the management of the patient.

Permanent dislocation in younger age can be

related with

many associated syndromes

;

whereas episodic dislocation is often isolated

but should consider connective tissues patholo­

gies when generalized hypermobility is noticed.

The figure 6 summarizes where to look at when

a clinician deal with patellar dislocation, aplasia

or hypoplasia.

In case of familial history or small patella, a

genetic disorder is suspected: parent’s assess­

ment, pelvis X-ray will be of major diagnosis

value (NPS, SPS and GPS).

And so the orthopedist surgeon will sometime

have to refer the patient to other specialist such

as geneticist, ophthalmologist, cardiologist, or

nephrologist…

Literature

[1] Bettuzzi C, Lampasi M, Magnani M,

and al.

Surgical treatment of patellar dislocation in children with

Down syndrome: a 3- to 11-year follow-up study.

Knee Surg

Sports Traumatol Arthrosc 2009; 17: 334-40.

[2] Bongers EM, Opitz JM, Fryer A,

and al.

Meier-

Gorlin syndrome: report of eight additional cases and review.

Am J Med Genet. 2001; 102: 115-24.

[3] Bongers EM, Van Bokhoven H, Van Thienen

MN,

and al.

The small patella syndrome: description of five

cases from three families and examination of possible

allelism with familial patella aplasia-hypoplasia and nail-

patella syndrome.

J Med Genet 2001; 38: 209-14.

[4] FerrellWR, Tennant N, Sturrock RD,

and al.

Ameliorationofsymptomsbyenhancementofproprioception

in patients with Joint hypermobility syndrome.

Arthritis and

Rheumatism 2004; 50: 332-28.

[5] Fleck BJ, Pandya A, Vanner L,

and al.

Coffin-

Siris syndrome: review and presentation of new cases from a

questionnaire study.

Am J Med Genet. 2001; 99: 1-7.

[6] Laville JM, Lakermance P, Limouzy F.

Larsen’s syndrome: review of the literature and analysis of

thirty-eight cases.

J Pediatr Orthop. 1994;14: 63-73.

[7] Leng HC, Foster P, Templeton PA. Fusion of

double-layered patella using a single small fragment partially

threaded screw: a case report.

J Pediatr Orthop 2011; 31: 9-12.

[8] Mehlman CT, Rubinstein JH, RoyDR. Instability

of the patellofemoral joint in Rubinstein-Taybi syndrome.

J Pediatr Orthop. 1998; 18: 508-11.

[9] Nomura E, Inoue M, Kobayashi S. Bilateral

recurrent patellar dislocation in a patient with isolated patella

aplasia-hypoplasia.

Arthroscopy. 2007; 23: 1136.e1-4.

[10] Remvig L, Jensen DV, Ward RC. Are diagnostic

criteria for general joint hypermobility and benign joint

hypermobility syndrome based on reproducible and valid tests

? A review of the literature.

J Rheumatol. 2007; 34:798-803.

[11] Shibata T, Kawabata H, Yasui N,

and al.

Correction of knee deformity in patients with Ellis-van

Creveld syndrome.

J Pediatr Orthop B. 1999; 8: 282-4.

[12] Sweeney E, Hoover-Fong JE, McIntosh I.

Nail-Patella Syndrome. In: Pagon RA, Bird TD, Dolan CR,

Stephens K,AdamMP, editors. GeneReviews™.

Seattle (WA):

University of Washington, Seattle; 1993-2003 [updated 2009].

[13] To M, Negandhi R, Cheung K,

and al.

Genitopatellar syndrome: a case report of a rare entity with

11 years of follow-up.

J Pediatr Orthop B 2012 May 6.