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CASE REPORT
Goltz syndrome: a rare case of father-to-daughter transmission
  1. Vishal Gupta1,
  2. Himabindu Saginatham1,
  3. Sudheer Arava2,
  4. Gomathy Sethuraman1
  1. 1Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India
  2. 2Department of Pathology, All India Institute of Medical Sciences, New Delhi, Delhi, India
  1. Correspondence to Professor Gomathy Sethuraman, aiimsgsr{at}gmail.com

Summary

An 8-year-old girl presented to us with skin-coloured to yellowish soft compressible papules, intermixed with hypopigmented and hyperpigmented macules in a Blaschkoid pattern, and ‘lobster-claw deformity’ affecting her bilateral feet. Additional examination findings included short stature, facial asymmetry, low-set ears, hypodontia, enamel hypoplasia, tonsillar enlargement and spina-bifida occulta at S1–3 vertebral level. A diagnosis of Goltz syndrome was suspected clinically, which was confirmed on skin biopsy. Her father also had hypopigmented and hyperpigmented macules in a Blaschkoid distribution, ‘lobster-claw’ deformity and kyphoscoliosis. None of the other family members were affected.

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