Foot hexadactyly, social implications and management in the African setting: Case report

Foot hexadactyly, social implications and management in the African setting: Case report

Hexadactyly of the foot, an abnormal congenital condition presenting aseight toes, is a rare malformation. We report the case of a ten-year-old girl,admitted to our orthopedic and reconstructive surgery department for a preaxialhexadactyly. The girl was abandoned by her parents at birth and stoppedschool early due to stigmatization. The goals of the surgical procedure were:social reintegration, gait improvement, ability to wear shoes comfortably, andimproved appearance of the foot. The surgery was a medial resection of thesupernumerary toes.

___

  • 1. Castilla EE, Lugarinho Da Fonseca R, da Graca Dutra M, Bermejo E, Cuevas L, Martinez-Frias ML. Epidemiological analysis of rare polydactylies. Am J Med Genet 1996; 65: 295-303.2
  • 2. Hwang K, Kim ET, Lee SI. Foot polydactyly and polysyndactyly: Genetic implications in two families. J Foot Ankle Surg 2005; 44: 473-477.
  • 3. Laurin CA, Favreau JC, Labelle P. Bilateral absence of the radius and tibia with bilateral reduplication of the ulna and fibula. A case report. J Bone Joint Surg Am 1964; 46: 137-142.
  • 4. Sandrow RE, Sullivan PD, Steel HH. Hereditary ulnar and fibular dimelia with peculiar facies. A case report. J Bone Joint Surg Am 1970; 52: 367-370.
  • 5. Skoll PJ, Silfen R, Hudson DA, Bloch CE. Mirror foot. Plast Reconstr Surg 2000; 105: 2086-2088.
  • 6. Bonnet F, Garrido I, Haddad R, Pavy B, Mitrofanoff M. Complex polydactyly of the limbs: Mirror foot. Report of two cases and review of literature. Ann Chir Plast Esthet 2005; 50: 323-327.
  • 7. El-Shazly M. An eight-toed foot: A rare pedal polydactyly. J Foot Ankle Surg 2007; 46: 207-209.
  • 8. Al-Qattan MM, Hashem FK, Al Malaq A. An unusual case of preaxial polydactyly of the hands and feet: A case report. J Hand Surg Am 2002; 27: 498-502.
  • 9. Dan U, Nayek K, Ghosh TN, Akhtar S. Complete tibial aplasia with preaxial polydactyly: A kindred of affected individuals in three generations. J Anat Soc India 2010; 59: 44-47.
  • 10. Wang HJ, Cheng LF, Tung YM, Chen TM. Centraltype eight-toed polydactyly associated with ipsilateral complex renogluteal agenesis: A case report with 8 years’ follow-up. J Pediatr Surg 1996; 31: 444-446.
  • 11. Johnson EJ, Neely DM, Dunn IC, Davey MG. Direct functional consequences of ZRS enhancer mutation combine with secondary long range SHH signalling effects to cause preaxial polydactyly. Dev Biol 2014; 392: 209-220.
  • 12. Han SH, Cho JH, Lee YS. An unusual case of postaxial polydactyly of the foot treated by metatarsal transfer. J Foot Ankle Surg 2014; 53: 59-61.
  • 13. Morley SE, Smith PJ. Polydactyly of the feet in children: Suggestions for surgical management. Br J Plast Surg 2001; 54: 34-38.
  • 14. Lui TH. Correction of postaxial metatarsal polydactyly of the foot by percutaneous ray amputation and osteotomy. J Foot Ankle Surg 2013; 52: 128-131.
Turkish Journal of Pediatrics-Cover
  • ISSN: 0041-4301
  • Yayın Aralığı: 6
  • Başlangıç: 1958
  • Yayıncı: Hacettepe Üniversitesi Çocuk Sağlığı Enstitüsü Müdürlüğü
Sayıdaki Diğer Makaleler

Oral health status in patients with mucopolysaccharidoses

ELİF BALLIKAYA, Pınar SERDAR EYMİRLİ, Yılmaz YILDIZ, Nihal AVCU, Hatice Serap SİVRİ, Meryem UZAMIŞ TEKÇİÇEK

A rare cause of facial nerve palsy in a young infant: Kawasaki disease

Ali ORGUN, Cüneyt KARAGÖL, Utku PAMUK, Hazım Alper GÜRSU, İlker ÇETİN

Response to ''Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition?''

Şahin Takcı, Şule Yiğit, Esra Serdaroğlu, Vineta Fellman

Apolipoprotein E allelic variants and cerebral palsy

Evren GÜMÜŞ, Beyhan DURAK ARAS, Oğuz ÇİLİNGİR, Coşkun YARAR, Kürşat Bora ÇARMAN, Sibel LAÇİNER GÜRLEVİK, Ozan KOÇAK, Sevilhan ARTAN

Foot hexadactyly, social implications and management in the African setting: Case report

Komla Sena Amouzou, Elodie Lucrece Joyce Malonga-Loukoula, Tete Edem Kouevi-Koko, Batarabadja Bakriga, Anani Abalo

An asthmatic child with allergic bronchopulmonary aspergillosis (ABPA)

Öner ÖZDEMİR

Venous thromboembolism in two adolescents with Down syndrome

Kei Takasawa, Masato Nishioka, Masayuki Shimohira, Reiko Takasawa, Sayaka Takeda, Masashi Kurobe, Tsunehiko Kurokami

Changes of primary headache related white matter lesions in pediatric patients

Erhan BAYRAM, Uluç YİŞ, Cem PAKETÇİ, Derya OKUR, İpek POLAT, Handan ÇAKMAKÇI, Semra HIZ, Banu ANLAR

Autism spectrum disorder and beta thalassemia minor: A genetic link?

Hamza AYAYDIN, Hatice TAKATAK

The association between monosymptomatic enuresis and allergic diseases in children

Caner Alparslan, Demet Alaygut, Suzan Yılmaz Durmuş, Seda Şirin Köse, Özden Anal, Alper Soylu