Popliteal Pterygium Syndrome (Facio-Genito-Popliteal Syndrome)
DOI:
https://doi.org/10.31907/2414-2093.2016.02.06Keywords:
Popliteal pterygium syndrome, Escobar syndrome, Magnetic resonance imaging, Congenital contractures, Genetic counseling.Abstract
Background: IRF6-related disorders span a spectrum from isolated cleft lip and palate and Van der Woude syndrome (VWS) at the mild end to popliteal pterygium syndrome (PPS) at the more severe end. Popliteal pterygia are found in popliteal pterygium syndrome, multiple pterygium syndrome and Arthrogryposis. The popliteal pterygium syndrome is a rare congenital condition, in which the patient has facial, genitourinary and skeletal anomalies along with popliteal pterygium. Autosomal dominant popliteal pterygium syndrome (AD-PPS) is a rare genetic malformation disorder characterized by cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. AD-PPS is associated with mutations in theIRF6gene (1q32.2-q32.3), involved in the formation of connective and epithelial tissues. Almost all affected patients harbor mutations in this gene. The word "pterygium" is derived from the Greek word pterygion, which means wing. Pathologically it denotes a wing-like abnormal band of tissue. The most obvious characteristics of this syndrome are popliteal pterygium and a triangular crease of skin over the hallux. The orofacial findings include cleft lip, cleft palate, lower lip pits, a few missing teeth, and severely decayed teeth. The dental problems are overshadowed by the major syndromic manifestations. These patients have special dental needs and early preventive dental care and appropriate dental treatment at the optimal time is important. Diagnosis of pterygium syndrome is based on the clinical findings and confirmed by molecular genetic testing. AD-PPS is highly associated with missense mutations that alter residues that are predicted to interact directly with DNA in exons 3 and 4 of IRF6.
Conclusion: An understanding of the molecular genetic basis of this syndrome is essential for prenatal diagnosis and also for genetic counseling of the parents.
References
Trelat U. Sur un vice conformation tres-rare de la levere - inflerieure. J Med Chir Prat. 1869; 40: 442-445.
Gorlin RJ, Sedano HO, Cervenka J. Popliteal pterygium syndrome. A syndrome comprising cleft lip palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics 1968; 41: 503-509.
Rintala A, Lahti A. The facio-genito-popliteal syndrome. Scand J Plast Reconstr Surg. 1970; 4: 67-71. http://dx.doi.org/10.3109/02844317009038446
Escobar V. Popliteal pterygium syndrome: A phenotypic and genetic analysis. J Med Genet. 1978; 15: 35-42. http://dx.doi.org/10.1136/jmg.15.1.35
Frohlich G. Popliteal pterygium syndrome: Report of a family. Pediatric 1977; 90: 91-93. http://dx.doi.org/10.1016/S0022-3476(77)80775-0
Spranger S, Spranger M, Meinck HM, Tariverdian G. Two sisters with Escobar syndrome. Am J Med Genet. 1995; 57(3): 425-428. http://dx.doi.org/10.1002/ajmg.1320570312
Deskin RW, Sawyer DG. Popliteal pterygium syndrome. Int J Pediatr Otorhinolaryngol. 1988; 15: 11-22. http://dx.doi.org/10.1016/0165-5876(88)90046-8
Schutte B. Microdeletions at the chromosome bands1q32- q41as a cause of van der woude syndrome. Am J Med Genet. 1999; 84:145-150. http://dx.doi.org/10.1002/(SICI)1096-8628(19990521)84:2< 145::AID-AJMG11>3.0.CO;2-L
Hunter A. The popliteal pterygium syndrome: Report of a new family and review of the literature. Am J Med Genet. 1990; 36: 196-208. http://dx.doi.org/10.1002/ajmg.1320360213
Bamshad M, Jorde LB, Carey JC. A revised and extended classification of the distal arthrogryposes. Am J Med Genet. 1996; 65: 277-281. http://dx.doi.org/10.1002/(SICI)1096-8628(19961111)65:4< 277::AID-AJMG6>3.0.CO;2-M
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, et al. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet. 2002; 32: 285-289. http://dx.doi.org/10.1038/ng985
Lees MM, Winter RM, Malcom S, Saal HM, Chitty L. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32. J Med Genet. 1999; 36: 888-892.
de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S, et al. Prevalence and non random distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genet Med. 2009; 11: 241- 247. http://dx.doi.org/10.1097/GIM.0b013e318197a49a
Leslie EJ, Standley J, Compton J, Bale S, Schutte BC, Murray JC. Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases. Genet Med. 2013; 15: 338-344. http://dx.doi.org/10.1038/gim.2012.141
Wu T, Liang KY, Hetmanski JB, Ruczinski I, Fallin MD, Ingersoll RG, et al. Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate. Hum Genet. 2010; 128: 401-410. http://dx.doi.org/10.1007/s00439-010-0863-y
Hecht F, Jarvinen JM. Heritable Dysmorphic syndrome with normal intelligence. J Pediatr. 1967; 70: 927-935. http://dx.doi.org/10.1016/S0022-3476(67)80265-8
Khans N. Intra familial variability of popliteal pterygium syndrome: A family description. Cleft Palate J. 1986; 23: 233-236.
Kind HP. Popliteales Pterygium-syndrom. Helv Paediatr Acta 1970; 25: 508-516.
Tuerk D, Edgerton MT. Thesurgical treatment ofcongenital webbing (pterygium) of the popliteal area. Plast Reconstrsurg. 1975; 56: 339-344. http://dx.doi.org/10.1097/00006534-197509000-00020
Addison A, Webb PJ. Flexion contractures of the knee associated with popliteal webbing. J Pediatr Orthoped. 1983; 3: 376-379. http://dx.doi.org/10.1097/01241398-198307000-00019
Champion R, Cregan JCF. Congenital popliteal webbing in siblings: Report of two cases. J Bone Joint Surg Br. 1969; 41: 355-359.
Basch K. Einweiterer Fallvonsog. Flughautbildung. Prag Medwschr. 1891; 16: 572-573 and 1892; 17: 287-291.
Baja PS, Bailey BM. Ectopic scrotum: A case report. Br J Plastsurg. 1969; 22: 87-89. http://dx.doi.org/10.1016/S0007-1226(69)80096-2
Aron NK. The popliteal web syndrome. Eur J Plastsurg. 1988; 11: 93-94. http://dx.doi.org/10.1007/BF00299222
Klein D. Uncurieux syndromehl erl editaire: Cheilo-palatoschizisavec"s-tulesdelal evreinfl erieureassocil eaunesyndactylie, uneonychodysplasieparti-culiere, unptl erygionpoplitl eunilatl eraleetdespiedsvarusl equins. J Genet Hum. 1962; 11: 65-71.
Pfeiffer RA. Das Kniepterygium-syndrom. Ein autosomal dominant vererbtes Missbildungssyndrom. Z Kinderheilkunde 1970; 108: 103-116. http://dx.doi.org/10.1007/BF00439878
Baruthcu A. A case with popliteal pterygium syndrome and its surgical treatment. Eur J Plastsurg. 1990; 13(4): 182-184. http://dx.doi.org/10.1007/BF00236376
Neuman Z, Shulman J. Congenital sinuses of the lower lip. Oral Surg. 1961; 14: 1415-1420. http://dx.doi.org/10.1016/0030-4220(61)90243-2
Gorlin RJ. Popliteal pterygium syndrome: A syndrome comprising cleft lip/palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics 1968; 41: 503-509.
Ozgur FF. Antecubital pterygium syndrome. Eur J Plastsurg. 1993; 16: 10-11.
Perrotin F. Prenatal ultrasonographic diagnosis of the popliteal pterygium syndrome. Prenat Diagn. 2000; 20: 501-504. http://dx.doi.org/10.1002/1097-0223(200006)20:63.0.CO;2-X
Oppenheim WL, Larson KR, McNabb MB, Smith CF, Setoguchi Y. Popliteal pterygium syndrome: an orthopaedic perspective. J Pediatr Orthop. 1990; 10(1): 58-64.
Gillen JA, Walker JL, Burgess RC, Stevens DB. Use of Ilizarov external fixator to treat joint pterygia. J Pediatr Orthop. 1996; 16(4): 430-7. http://dx.doi.org/10.1097/01241398-199607000-00003
Parikh SN, Crawford AH, Do TT, Roy DR. Popliteal pterygium syndrome: implications for orthopaedic management. J Pediatr Orthop B. 2004; 13(3): 197-201.
Bartsocas CS, Papas CV. Popliteal pterygium syndrome: evidence for a severe autosomal recessive form. J Med Genet. 1972; 9(2): 222-6. http://dx.doi.org/10.1136/jmg.9.2.222
Giannotti A, Digilio MC, Standoli L, Zama M, Dallapiccola B. New case of Bartsocas-Papas syndrome surviving at 20 months. Am J Med Genet. 1992; 42(5): 733-5. http://dx.doi.org/10.1002/ajmg.1320420522
Hoffmann K, Muller JS, Stricker S, Megarbane A, Rajab A, Lindner TH, et al. Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit. Am J Hum Genet. 2006; 79(2): 303- 312. http://dx.doi.org/10.1086/506257
Michalk A, Stricker S, Becker J, Rupps R, Pantzar T, Miertus J, et al. Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. Am J Hum Genet. 2008; 82(2): 464-76. http://dx.doi.org/10.1016/j.ajhg.2007.11.006
Morgon NV, Brueton LA, Cox P, Tolmie J, Pasha S, Morton JE. Mutations in the embryonal subunits of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome. Am J Hum Genet. 2006; 79(2): 390-395. http://dx.doi.org/10.1086/506256
Herold HZ, Shmueli G, Baruchin AM. Popliteal pterygium syndrome. Clin Orthop Relat Res. 1986; 209: 194-7. http://dx.doi.org/10.1097/00003086-198608000-00027
McCall RE, Budden J. Treatment of multiple pterygium syndrome. Orthopedics 1992; 15(12): 1417-22.
Matolcsy T. Ueber die chirurgische Behandlung der angeborenen Flughhaut. Langenbeck Arch Klin Chir 1936; 185: 675- 681.
Srivastava RN. Arthrogryposis multiplex congenita: Case reports of two siblings. Clin Pediatr. 1968; 7: 691-4. http://dx.doi.org/10.1177/000992286800701112
Gorlin RJ, Cohen MM, Hennekam RC. Chromosomal syndromes: Common and/or well-known syndromes. Syndromes of the Head and Neck (4th ed). Oxford:Oxford University Press; 2001; 62-66.
Celikoz B. A variant of Noonan’s syndrome. Eur J Plast Surg. 1997; 20: 157-560. http://dx.doi.org/10.1007/BF01002053
Thompson EM, Donnai D, Baraitser M, Hall CM, Pembrey ME, Fixsen J. Multiple pterygium syndrome evolution of the phenotype. J Med Genet. 1987; 2(4): 733-49. http://dx.doi.org/10.1136/jmg.24.12.733
Herzenberg JE, Davis JR, Paley D, Bhave A. Mechanical distraction for treatment of severe knee fl exion contractures. Clin Orthop Relat Res. 1994; 301: 80-8.
Saleh M, Gibson MF, Sharrard WJ. Femoral shortening in correction of congenital knee flexion deformity with popliteal webbing. J Pediatr Orthop. 1989; 9(5): 609-11. http://dx.doi.org/10.1097/01241398-198909010-00020
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