Literature DB >> 12657010

Collodion baby associated with asymmetric crying facies: a case report.

Mustafa Akcakus1, Tamer Gunes, Selim Kurtoglu, Adnan Ozturk.   

Abstract

Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a variety of underlying abnormalities. The phenotype includes parchment-like hyperkeratosis, pseudocontractures, ectropion, eclabium, absence of eyebrows, and sparse hair. Asymmetric crying facies is caused by congenital hypoplasia or agenesis of the depressor anguli oris muscle. Associations of this facial defect with major congenital anomalies have been reported, most commonly in the cardiovascular system, less frequently involving the genitourinary, musculoskeletal, cervicofacial, and respiratory systems, and rarely the endocrine system. We report a newborn with a collodion membrane and asymmetric crying facies. To the best of our knowledge, this association has not been previously published.

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Year:  2003        PMID: 12657010     DOI: 10.1046/j.1525-1470.2003.20208.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  2 in total

1.  Facial Asymmetry in a Newly Born Baby: Diagnostic Challenge!

Authors:  Naglaa M Kamal; Maher Mr Omair; Ruwayd Attar; Salma As Abosabie; Nawras M Asiri; Laila M Sherief; Mortada El-Shabrawi
Journal:  Clin Med Insights Case Rep       Date:  2022-03-28

2.  Collodion Baby with TGM1 gene mutation.

Authors:  Deepak Sharma; Basudev Gupta; Sweta Shastri; Aakash Pandita; Smita Pawar
Journal:  Int Med Case Rep J       Date:  2015-09-22
  2 in total

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