Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Complete and homogenous trisomy 9 detected in utero].

Journal de gynecologie, obstetrique et biologie de la reproduction - 1 Jan 1992

Raffi F, Geneix A, Satge D, Fallouh B, Brunerie A M, Lemery D, Malet P

Abstract excerpt

During a gestation with oligoamnios and growth retardation noticed at 25th week an amniocentesis allowed us to discover the 14th case of complete trisomy 9, the third detected in utero. It is also the first without heart malformation, otherwise phenotype was usual. The liver had small areas of necrosis with calcifications and slight fibrosis which may be in relation with two cordocentesis made before expulsion....

Topics

Abortion, Therapeutic
Adult
Amniocentesis
Chromosomes, Human, Pair 9
Female
Fetal Growth Retardation
Humans
Infant, Newborn
Karyotyping
Liver Diseases
Male

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Oligohydramnios

Phenotype

Prenatal Diagnosis

Trisomy

Source

Identifiers

PMID: 1583306

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1583306-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Complete and homogenous trisomy 9 detected in utero].PMID 1583306Read ↗

[Fetal phenotypic aspects of trisomy 18. 9 cases diagnosed prenatally].Semantic proximity Read ↗

[Partial trisomy 9p syndrome: Expanding the phenotype].Semantic proximity Read ↗

Trisomy 18: experience of a reference hospital from the south of Brazil.Semantic proximity Read ↗

[Mosaic trisomy of chromosome 20 in a patient with congenital anomalies--10-years observation].Semantic proximity Read ↗

Rare case of live born with confirmed mosaic trisomy 17 and review of the literatureSemantic proximity Read ↗

Prenatal diagnosis of fetal trisomy 6 mosaicism and phenotype of the affected newborn.Semantic proximity Read ↗

Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancySemantic proximity Read ↗

[Mosaic trisomy 9: report of a new case with a long-term survival].Semantic proximity Read ↗

[Apolipoprotein E and fetal trisomies].Semantic proximity Read ↗

[Monosomy 9p. Clinical and cytogenetic aspects].Semantic proximity Read ↗

Trisomy 16 in a mid-trimester IVF foetus with multiple abnormalities.Semantic proximity Read ↗

[Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.