Indian Journal of Medical Research

CLINICAL IMAGE
Year
: 2014  |  Volume : 139  |  Issue : 6  |  Page : 963--964

Gollop-Wolfgang syndrome


Naresh Dhanakodi, Sujit Kumar Tripathy 
 Deparment of Orthopedics, Meenakshi Mission Hospital & Research Center, Madurai 625 107, India

Correspondence Address:
Sujit Kumar Tripathy
Deparment of Orthopedics, Meenakshi Mission Hospital & Research Center, Madurai 625 107
India




How to cite this article:
Dhanakodi N, Tripathy SK. Gollop-Wolfgang syndrome.Indian J Med Res 2014;139:963-964


How to cite this URL:
Dhanakodi N, Tripathy SK. Gollop-Wolfgang syndrome. Indian J Med Res [serial online] 2014 [cited 2020 Aug 12 ];139:963-964
Available from: http://www.ijmr.org.in/text.asp?2014/139/6/963/138101


Full Text

A 3-month old male child was brought to the Orthopaedics department of Meenakshi Mission Hospital and Research Center, Madurai, Tamil Nadu, India, in October 2012 with complaints of multiple lower limb and upper limb deformities. On clinical examination, bilateral club feet and abnormal prominence in the left thigh were found [Figure 1]. In the upper limbs, the child had lobster-claw shaped hand on both sides. Radiographs confirmed the prominence of left thigh as a 'bifid femur' [Figure 2]. Right tibia was partially formed (tibial hemimelia). Absence of central rays of hands was found on both sides (ectrodactyly) [Figure 3]. The child was evaluated and not found to have any visceral and congenital cardiac anomalies. {Figure 1}{Figure 2}{Figure 3}

The combination of tibial hemimelia, ectrodactyly, bifid-femur and split hand comprises the features of Gollop-Wolfgang complex. Excision of left sided bifurcated femur and right limb knee disarticulation with prosthesis was advised, but the parents of the child refused. The parents revisited the outpatient department in January 2013, but did not give consent for the above treatment.