Collodion Baby with TGM1 gene mutation

Collodion baby (CB) is normally diagnosed at the time of birth and refers to a newborn infant that is delivered with a lambskin-like membrane encompassing the total body surface. CB is not a specific disease entity, but is a common phenotype in conditions like harlequin ichthyosis, lamellar ichthyos...

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Detalles Bibliográficos
Autores principales: Sharma, Deepak, Gupta, Basudev, Shastri, Sweta, Pandita, Aakash, Pawar, Smita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590349/
https://www.ncbi.nlm.nih.gov/pubmed/26451124
http://dx.doi.org/10.2147/IMCRJ.S91517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590349/
https://www.ncbi.nlm.nih.gov/pubmed/26451124
http://dx.doi.org/10.2147/IMCRJ.S91517

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