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Related Experiment Video

Updated: May 8, 2026

Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy

Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy

Published on: August 25, 2019

Potter's Sequence.

Srikanth M Shastry¹, Sachin S Kolte, Panduranga R Sanagapati

¹Department of Pathology, Mamata Medical College, Khammam, Andhra Pradesh, India.

Journal of Clinical Neonatology

|September 13, 2013

Summary

This summary is machine-generated.

Potter

Keywords:

Potter facies pulmonary hypoplasia renal agenesis

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Area of Science:

Medical genetics
Developmental biology
Pediatric pathology

Background:

Potter's sequence is a rare, fatal congenital disorder.
It presents in sporadic and autosomal recessive forms.
Incidence is approximately 1 in 4000 births.

Observation:

Affected neonates often exhibit stillbirth or early neonatal demise.
This case report details a patient with characteristic physical manifestations.
Histological examination revealed typical pathological findings.

Findings:

The case presented with classic physical signs of Potter's sequence.
Histopathological analysis confirmed the diagnosis.
This aligns with known presentations of the disorder.

Implications:

Highlights the importance of recognizing Potter's sequence in neonates.
Contributes to the understanding of its genetic and pathological basis.
Informs clinical management and genetic counseling for affected families.