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Lehman syndrome

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Lehman syndrome" returned 1 free, full-text review articles. First 1 results:
The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).
Last Updated: Nov 17, 2011

Börjeson-Forssman-Lehman syndrome was first described in 1962. Many similar families and isolated cases have been reported since. In nineteen of them, including the original family, the clinical diagnosis was confirmed by the identification of a mutation in the responsible gene, ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Lehman syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Lehman syndrome" returned 0 free, full-text research articles. First 0 results:
Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.
Last Updated: Dec 30, 2016

Lateral meningocele syndrome (LMS), or Lehman syndrome, is a rare disorder characterized by multiple lateral spinal meningoceles, distinctive facial features, joint hypermobility and hypotonia, along with skeletal, cardiac, and urogenital anomalies. Heterozygous NOTCH3 mutations affecting ...

Lehman syndrome: a new syndrome for pierre robin sequence.
Last Updated: Feb 01, 2018

Lehman syndrome, or lateral meningocele syndrome, is characterized by facial dysmorphism, multiple lateral meningoceles, and skeletal abnormalities. Only nine cases have been described. We present a case of a 2-year-old boy presenting with micrognathia, glossoptosis, and hypertelorism ...

Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome.
Last Updated: Nov 01, 2019

We describe a 19-year-old boy who presented with facial dysmorphism, multiple lateral meningoceles, skeletal abnormalities and normal intelligence. Neurofibromatosis and Marfan syndrome were excluded. Electron microscopy of the skin showed non-specific abnormalities suggesting a connective ...

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