Paediatric Limb Deficiency

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Introduction[edit | edit source]

Limb deficiencies can be defined as a part or entire upper or lower limb failed to form its normal size or is missing. It can be classified into two:

  1. Congenital and
  2. Acquired.

Congenital limb deficiencies can involve upper or lower limb, at birth due to several factors although the exact cause is unknown.Approximately 58% congenital limb deficiencies involving upper limb. Longitudinal deficiency [1] of hand and transverse below elbow limb deficiency are the most common presentation with 20% of children present with limb deficiencies affecting more than one limb. On the other hand,proximal femoral focal deficiency (PFFD) [2] is a term for complex lower extremity congenital limb deficiency. It may be unilateral or bilateral, which includes the absence of proximal femur involving the acetabulum, femoral head, patella, tibia and fibula. Both Aitken [3] and Gillespie have developed a classification [4] for PFFD based on severity and complexity of medical intervention respectively. Another 40% of childhood amputation is acquired amputations involving trauma and disease-related.

Classification[edit | edit source]

Various classification has been developed to congenital limb deficiencies. However,Swanson [5] and colleagues have modified the classification based on embryonic failure:-

  1.  Failure of formation of parts
  2.  Failure of differentiation of parts
  3. Duplication
  4. Overgrowth
  5. Undergrowth
  6. Congenital constriction band syndrome
  7. Generalized skeletal deformities

Causes
[edit | edit source]

  • Familial inheritance
  • Chromosomal abnormality
  • Poor nutrition
  • Vascular disruption to the limbs
  • Drug/alcohol abuse & during pregnancy
  • Exposure to certain medications/chemicals
  • Asymmetric neurological disorders (E.g. Poliomyelitis, encephalopathy, etc)
  • Trauma
  • Growth plate disturbances (E.g. Infection, tumor)
  • Soft tissue overgrowth

Types[edit | edit source]

According to the ISO/ISPO classification [6], the anatomic and radiologic bases are used to describe the congenital limb deficiency. It consists of:-

  1. Longitudinal deficiencies : 
  •  Absence or reduction of an element or elements happens within the long axis of the limb.
  • About two thirds of the cases are associated with other congenital anomalies such as Adams-Oliver, Holt Oram, Poland, Fanconi, and VACTERL syndrome.

     2. Transverse deficiencies :

  • Limb has developed normally until certain level where skeletal elements are absent, though there may be digital buds.
  • Most common cause is amniotic bands while the remaining cases are mostly due to underlying genetic syndromes.


Approximately 70%-85% of acquired amputation is due to trauma and the remaining is the result of disease.

  1. Traumatic amputation
  • Incidence vary according to age and geographic location.
  • Farm machinery and household power tools are the leading factors to traumatic amputation.
  • Amputation due to motor vehicle accidents, gunshot wounds and railroad accidents are common in older child.

    2. Disease-related amputation
  • In children, it is rare for primary bone tumors to occur.
  • However, the most common primary bone tumors are osteosarcoma and Ewing’s sarcoma.

Sign and Symptom[edit | edit source]

General (whereby both congenital and acquired facing similar difficulties)[edit | edit source]

  1.  Loss of skeletal component
  2. Delay normal motor development
  3. Assistance with daily activities such as self-care
  4. Potential emotional and social issues because of physical appearance

Congenital[edit | edit source]

  1. Limb length discrepancy
  2. Other associated musculoskeletal abnormalities

Acquired[edit | edit source]

  1. Phantom sensation : A tingling sensation that felt by the patient as if the part amputated is still present.
  2. Phantom pain: Pain that exist after an amputation which appears in burning, aching, shooting or any other characterization.

Diagnosis & Tests[edit | edit source]

  • Prenatal ultrasound
  • Genetic tests
  • Physical examinations
  • X ray
  • MRI


Typically, x-rays are done to determine which bones are involved. When defects appear to be familial or if a genetic syndrome is suspected, evaluation should also include a thorough assessment for other physical, chromosomal, and genetic abnormalities. When available,assessment by a clinical geneticist is useful.

Medical Management[edit | edit source]

The medical management is divided into :-

Congenital[edit | edit source]

UL[edit | edit source]

  1. Amputation
  • Shoulder disarticulation
  • Forearm amputation
  • Hand amputation

LL[edit | edit source]

  1. Tenotomy
  2. Amputation
  • Hip disarticulation
  • Transfemoral amputation
  • Transtibial amputation
  • Ankle and foot disarticulation
  • Syme’s amputation or Boyd amputation
  • Partial foot amputation and tenotomy
  • Chopart (Mid-tarsal joint)
  • Lisfranc (Tarsometatarsal joint)

     3.  Prosthetic


Acquired[edit | edit source]

UL and LL[edit | edit source]

  1. Amputation
  2. Prosthetic

Physiotherapy Management[edit | edit source]

It is important for the child to attend physiotherapy treatment to facilitate as normal development sequence as possible. Besides, development of impairments and activity limitations should be prevented or minimized. However, there are several factors that might influence the intensity of physiotherapy needed which are child’s age, type of limb deficiency, level of amputation and other medical factors.
Functional abilities of the child can be highlighted through the examination of neuromotor development, aerobic capacity and endurance, gait and balance, community and work integration, and self care. Overall goals of a physiotherapist are:-

  • Prevent joint contracture
  • Minimize muscle strength imbalances
  • Prevent skin breakdown
  • Develop independence with mobility and self-care skills

In addition, meeting among the children, parents, teachers and physiotherapists before the beginning of the school may be helpful to allay any concerns and to develop a way to answer the questions of the child’s peers.

Outcome Measure[edit | edit source]

The Child Amputee Prosthetics Project- Functional Status Inventory (CAPP-FSI) was developed to assess 40 activities on two scales to determine whether the child performs the activity with or without prosthesis. A recently developed functional outcome measure, Functional Mobility Assessment (FMA), comprises six categories:-

  1. pain
  2.  function as measured by timed up and down stairs (TUGS) and the timed up and go (TUG) Timed_Up_and_Go_Test_(TUG)
  3. use of supports or assistive devices
  4. satisfaction with quality of walking
  5. participation in work, school, and sports
  6. endurance as measured by a 6 minute walk test _6_Minute_Walk_Test

References[edit | edit source]

 

  1. Abdel-Mota’al M., 201-. Proximal Femoral Focal Deficiency. Available at:< http://gait.aidi.udel.edu/educate/pffd.htm> [Accessed 3 February 2015]
  2. Lee M.C., 2014. Proximal Femoral Focal Deficiency. Medscape. [website] Available at:< http://emedicine.medscape.com/article/1248323-overview#a0101> [Accessed 3 February 2015]
  3. Aitken, G.T.: Congenital short femur with fibular hemimelia. JBJS: 56 -A: 1306, 1974
  4. Skalski M., et al., 201-. Classification of Proximal Focal Femoral Deficiency. Radiopeadia.org [website] Available at:< http://radiopaedia.org/articles/classification-of-proximal-focal-femoral-deficiency> [Accessed 3 February 2015]
  5. Swanson A.B., 1976. A Classification for Congenital Limb Malformations. PubMed. [website] Available at:< http://www.ncbi.nlm.nih.gov/pubmed/1021591> [Accessed 4 February 2015]
  6. Day H.J., 1991. The ISO/ISPO Classification of Congenital Limb Deficiency. PubMed. [website] Available at:< http://www.ncbi.nlm.nih.gov/pubmed/1923724> [Accessed 4 February 2015]