Literature DB >> 27530877

Goltz syndrome: a rare case of father-to-daughter transmission.

Vishal Gupta1, Himabindu Saginatham1, Sudheer Arava2, Gomathy Sethuraman1.   

Abstract

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. 2016 BMJ Publishing Group Ltd.

Entities:  

Mesh:

Year:  2016        PMID: 27530877      PMCID: PMC5015142          DOI: 10.1136/bcr-2016-216599

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  11 in total

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  1 in total

1.  Unilateral Focal Dermal Hypoplasia (Goltz Syndrome): Case Report and Literature Review.

Authors:  Sahar Alsharif; Sohad Hindi; Fay Khoja
Journal:  Case Rep Dermatol       Date:  2018-05-03
  1 in total

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