Literature DB >> 28272663

Neu-Laxova Syndrome: An Unusual Association with Kyphosis.

Amandeep Kaur1, Vijayalaxmi Suranagi, Kamal Patil, Hema Bannur.   

Abstract

The Neu-Laxova syndrome is a rare autosomal recessive condition associated with neuro-ectodermal abnormalities and other patterns of severe malformations leading to prenatal or early postnatal lethality. Association with kyphosis is an extremely rare finding. A fetus born from a 25-year-old gravida at 30 weeks gestation was diagnosed with Dandy Walker syndrome with severe intrauterine growth restriction on ultrasonography. On post-mortem examination after termination of pregnancy, the fetus showed facial dysmorphology with microcephaly, smooth shiny skin and kyphosis. Skin histology showed hyperkeratosis, edema and increased subcutaneous fat suggestive of ichthyosis. On the basis of gross and microscopic features seen, a diagnosis of Neu-Laxova syndrome was made.

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Year:  2018        PMID: 28272663     DOI: 10.5146/tjpath.2015.01353

Source DB:  PubMed          Journal:  Turk Patoloji Derg        ISSN: 1018-5615


  2 in total

Review 1.  Prenatal Diagnosis of Neu-Laxova Syndrome.

Authors:  Adriana Serrano Olave; Alba Padín López; María Martín Cruz; Susana Monís Rodríguez; Isidoro Narbona Arias; Jesús S Jiménez López
Journal:  Diagnostics (Basel)       Date:  2022-06-23

Review 2.  Microcephaly in Neurometabolic Diseases.

Authors:  Wiktoria Kempińska; Karolina Korta; Magdalena Marchaj; Justyna Paprocka
Journal:  Children (Basel)       Date:  2022-01-11
  2 in total

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