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present case surgical intervention was undertaken at
                                                              6 years of age, albeit with a good outcome.
                                                              The cleft closure is achieved by excision of excess tissue
                                                              including the third metacarpal and transverse bone bar
                                                              if present. To hold the diverging metacarpals together,
                                                              numerous techniques have been employed, such as heavy
                                                              chromic catgut sutures or stainless steel wires, the latter
                                                              done in the present case.  For the restoration of the first
                                                                                   [12]
                                                              web space, Snow and Littler advocated syndactyly release
                                                              and utilization of skin from the palmar side.  Barsky et al.
                                                                                                   [13]
                                                              employed a diamond-shaped flap from the cleft area itself
                                                              to create a web space.  In our case, the first web space
                                                                                  [12]
                                                              was created surgically in the right hand by simple closure
                                                              with a series of Z-plasties. The child may require rotational
                                                              osteotomies of the metacarpals, especially the marginal ones,
          Figure 5: Functional and cosmetic outcome 1 year after surgery
                                                                                                             [12]
                                                              to achieve a useful pincer grasp if not restored adequately.
                                                              No such procedure was done in this case as the patient and
          Contraction of the first web space and limitation of thumb   relatives were satisfied with the primary surgery outcome.
          adduction is the main functional handicap encountered in   Surgery for cleft foot is rarely required for hallux valgus
          such cases, based on which Manske and Halikis devised a   correction and still rarer for cosmetic reasons. [14]
          severity classification. [11]
                                                              Typical and atypical cleft hand deformities occur with
          Numerous clinical associations of SHFM have been    varying degrees of severity. Children learn to adapt
          documented; cleft lip/palate seems to be a consistent   from an early age and frequently develop remarkable
          accompanying manifestation. Such manifestations pose   functionality. If surgery is to be done, it should be planned
          airway difficulties which can lead to a potential higher   carefully for each patient. The aim of surgery in these
          morbidity and mortality. The constellation of findings   cases is mostly cosmetic. Any surgical procedure done
          most commonly reported is ectrodactyly ectodermal   should not jeopardize existing functions of the hand.
          dysplasia cleft lip/palate syndrome – ectrodactyly (SHFM),
          ectodermal dysplasia (coarse dry skin, glandular
          abnormalities), and cleft lip/palate. In the present case,         REFERENCES
          a thorough search was made for associated systemic
          anomalies, but fortunately none were observed. Sporadic,   1.   Bajwa SJ, Kulshrestha A, Kaur J, Gupta S, Singh A, Parmar SS. The challenging
                                                                  aspects and successful anaesthetic management in a case of situs inversus
          isolated, bilateral typical cleft hand as reported above is   totalis. Indian J Anaesth 2012;56:295-7.
          indeed a rare entity.                               2.   Kulshrestha A, Bajwa SJ, Singh A, Kapoor V.   Dexmedetomidine and fentanyl
                                                                  combination for procedural sedation in a case of Duchenne muscular
          Clinical diagnosis of SHFM is quite straightforward.    dystrophy.      Anesth Essays Res 2011;5:224-6.
          Although there is no evidence in the literature regarding   3.   Bajwa SJ, Gupta S, Kaur J, Panda A, Bajwa SK, Singh A, Parmar SS, Prasad S.
          differences in outcome for patients presenting as       Anesthetic considerations and diffi cult airway management in a case of
                                                                  Noonan syndrome. Saudi J Anaesth 2011;5:345-7.
          syndromic cases or in isolation, the associated anomalies   4.   Bajwa SJ, Bajwa SK, Singh A, Khan B, Parmar SS, Singh G, Kaur J. Anesthetic
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          biopsy is not a useful tool even if manifestations of       Unilateral cleft hand (lobster-claw deformity): a case report. J   Chin Clin Med
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          ectodermal dysplasia are absent, as done by some    6.   Baba AN, Bhat YJ, Ahmed SM, Nazir A. Unilateral cleft hand with cleft foot.
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          guide decision-making.                              7.   Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S,
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          Basic treatment goals are cleft closure for cosmetic    Naritomi K, Hughes H, Genuardi M, Gurrieri F, Neri G, Lovrein E, Magenis E,
          reasons, syndactyly release, and restoration of the first   Tsui LC, Evans JP. Fine mapping of the autosomal dominant split hand/
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                                                                  1994;55:12-20.
          functional impairment can be left untreated. Other   8.   Gurrieri F, Prinos P, Tackels D, Kilpatrick MW, Allanson J, Genuardi M,
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          the cosmetic appearance of the limb and the overall     Tsipouras P. A split hand-split foot (SHFM3) gene is located at 10q24-->25.
          psychology of the child. The ideal time for scheduling   9.   Am J Med Genet 1996;62:427-36.
                                                                  Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ,
          corrective surgery is at 18 months of age. The advantages   Yang-Feng TL. Deletion of chromosome 2q24-q31 causes characteristic
          of early surgery seem to be a correction of the deformity   digital anomalies: case report and review. Am J Med Genet 1995;55:155-60.
          before the development of refined motor skills and the   10.  Jones NF, Kono M. Cleft hands with six metacarpals.  J  Hand Surg Am
                                                                  2004;29:720-6.
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