Fibular hemimelia

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Fibular hemimelia
Other namesLongitudinal fibular deficiency
Amphibian hemimelia.jpg
Hemimelia in an amphibian affecting both calf and foot on one side
SpecialtyMedical genetics, orthopedics

Fibular hemimelia or longitudinal fibular deficiency is "the congenital absence of the fibula and it is the most common congenital absence of long bone of the extremities."[1][2] It is the shortening of the fibula at birth, or the complete lack thereof. In humans, the disorder can be noted by ultrasound in utero to prepare for amputation after birth or complex bone lengthening surgery. The amputation usually takes place at six months with removal of portions of the legs to prepare them for prosthetic use. The other treatments which include repeated corrective osteotomies and leg-lengthening surgery (Ilizarov apparatus) are costly and associated with residual deformity.[3]


Bones of human lower extremity

Characteristics are:

  • A fibrous band instead of the fibula
  • Short deformed leg
  • Absence of the lateral part of the ankle joint (due to absence of the distal end of the fibula), and what is left is unstable; the foot has an equinovalgus deformity
  • Possible absence of part of the foot requiring surgical intervention to bring the foot into normal function, or amputation.
  • Possible absence of one or two toes on the foot
  • Possible conjoined toes or metatarsals

Partial or total absence of fibula is among the most frequent limb anomalies. It is the most common long bone deficiency and is the most common skeletal deformity in the leg. It most often is unilateral (present only on one side). It may also present as bilateral (affecting both legs). Paraxial fibular hemimelia is the most common manifestation in which only the postaxial portion of the limb is affected. It is commonly seen as a complete terminal deficiency, where the lateral rays of the foot are also affected. Hemimelia can also be intercalary in which case the foot remains unaffected. Although the missing bone is easily identified, this condition is not simply a missing bone.[2] Males are affected twice as often as females in most series.[clarification needed][4]


The cause of fibular hemimelia is unclear. Purportedly, there have been some incidents of genetic distribution in a family;[citation needed] however, this does not account for all cases. Maternal viral infections, embryonic trauma, teratogenic environmental exposures or vascular dysgenesis (failure of the embryo to form a satisfactory blood supply) between four and seven weeks gestation are considered possible causes.[5]

In an experimental mouse model, change in the expression of a homeobox gene led to similar, but bilateral, fibular defects.[6]

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  1. ^ Eze, KC; Akhigbe, AO; Awosanya, GO (2007). "Fibular hemimelia: A case report". Nigerian Journal of Clinical Practice. 10 (3): 259–61. PMID 18072458.
  2. ^ a b Achterman, C; Kalamchi, A (May 1979). "Congenital deficiency of the fibula". The Journal of Bone and Joint Surgery. British Volume. 61-B (2): 133–37. doi:10.1302/0301-620X.61B2.438260. PMID 438260.
  3. ^ Stanitski, DF; Stanitski, CL (2003). "Fibular hemimelia: A new classification system". Journal of Pediatric Orthopedics. 23 (1): 30–34. doi:10.1097/01241398-200301000-00006. PMID 12499939.
  4. ^ "Fibular Hemimelia: (longitudinal fibular deficiency) – Wheeless' Textbook of Orthopaedics". 2011-03-30. Retrieved 2012-08-03.
  5. ^ "Fibular Hemimelia". Retrieved 2013-02-24.
  6. ^ Papenbrock, T; et al. (2000). "Loss of fibula in mice overexpressing Hoxc11". Mechanisms of Development. 92 (2): 113–23. doi:10.1016/S0925-4773(99)00344-5. PMID 10727851.

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