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As such, articles are written and edited by fetus net contributing members over a period of time. A global group of dedicated editors oversee accuracy, consulting with expert advisers, and constantly reviewing additions. Create new articleUpdating… Please wait. Article 18q-deletion syndrome is a rare chromosomal anomaly fetus net there is a deletion of part of the long arm of chromosome 18. Associated symptoms and findings vary widely, as fetus net their severity.

Characteristic clinical features include short fetus net, intellectual disability, hypotonia, facial, and dist. Article 1p36 deletion syndrome, or monosomy 1p36, is a chromosomal abnormality characterized most commonly by a deletion in the distal segment of the short arm of chromosome one 1.

Epidemiology The 1p36 deletion syndrome is present in approximately 1 in 5,000 live births. It is the most common termina.

Article 4D syndrome is a term fetus net to describe a manifestation of syndromic glucagonoma, a type of pancreatic endocrine tumor.

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