Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf
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Descrição
Cornelia de Lange syndrome (CdLS) encompasses a spectrum of findings from mild to severe. Severe (classic) CdLS is characterized by distinctive facial features, growth restriction (prenatal onset; <5th centile throughout life), hypertrichosis, and upper-limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly (missing digits). Craniofacial features include synophrys, highly arched and/or thick eyebrows, long eyelashes, short nasal bridge with anteverted nares, small widely spaced teeth, and microcephaly. Individuals with a milder phenotype have less severe growth, cognitive, and limb involvement, but often have facial features consistent with CdLS. Across the CdLS spectrum IQ ranges from below 30 to 102 (mean: 53). Many individuals demonstrate autistic and self-destructive tendencies. Other frequent findings include cardiac septal defects, gastrointestinal dysfunction, hearing loss, myopia, and cryptorchidism or hypoplastic genitalia.
Wiedemann-Steiner Syndrome - GeneReviews® - NCBI Bookshelf
Clinical Diagnosis of Classical Cornelia de Lange Syndrome Made From Postmortem Examination of Second Trimester Fetus With Novel NIPBL Pathogenic Variant - Jennifer Hague, Philip Twiss, Zoe Mead, Soo-Mi Park, 2019
Figure 1. [Characteristic facial dysmorphisms in CDK13]. - GeneReviews® - NCBI Bookshelf
Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 – topic of research paper in Clinical medicine. Download scholarly article PDF and read for
Children, Free Full-Text
Figure 2. [Hands of a woman age]. - GeneReviews® - NCBI Bookshelf
De Lange Syndrome
Cornelia de Lange syndrome in diverse populations - Dowsett - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library
Cornelia de Lange Syndrome: insights into neural development from clinical studies and animal models - ScienceDirect
Cornelia de Lange Syndrome: A Variable Disorder of Cohesin Pathology
De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females
Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7
Figure 3. [Range of limb anomalies in CdLS]. - GeneReviews® - NCBI Bookshelf
Figure 2. [Four individuals with Emanuel syndrome]. - GeneReviews® - NCBI Bookshelf
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
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