A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype

• Main Authors: Deepa Banker (Author), Bhavdeep Mungala (Author), Zankhana Parekh (Author), Shachi Ganatra (Author), Vimal Maheshwari (Author), Yashica Raj (Author), Utsav Patel (Author), Digant Patel (Author), Kishan Chamar (Author), Vasu Solanki (Author)
• Format: Book
• Published: Hindawi Limited, 2023-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Microdeletion of the short arm of chromosome 18 is one of the most common chromosome deletion syndromes. Its estimated frequency is 1 in 50,000 live-born infants, with female prevalence over males. Around 150 cases have been described till now. The reported abnormalities include growth deficiency, h...