Discover Community Create You

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

Prenatal diagnosis of Apert syndrome with widely separated cranial sutures.

Prenatal diagnosis - 1 Mar 2000

Lyu K J, Ko T M

Abstract excerpt

A 35-year-old Taiwanese woman visited us for prenatal evaluation in the 20th week of pregnancy. Both clinical observation of the mother and analysis of maternal DNA indicated a diagnosis of Apert syndrome. Sonographic examination of the fetus demonstrated findings that were consistent with this diagnosis; however, no prematurely fused cranial sutures were observed. The pregnancy was terminated after genetic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acrocephalosyndactylia
Share to Base Sequence
Share to Cranial Sutures

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gestational Age

Share to Pregnancy

Share to Receptors, Fibroblast Growth Factor

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 10719333

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis of Apert syndrome with widely separated cranial sutures.PMID 10719333Read ↗

Prenatal diagnosis of Apert syndrome caused by a de novo FGFR2 mutation in the second trimester: a case report.Semantic proximity Read ↗

Apert syndrome: A case report of prenatal ultrasound, postmortem cranial CT, and molecular genetic analysis.Semantic proximity Read ↗

Prenatal diagnosis and management of Apert syndrome in a low-middle income country: Case reportSemantic proximity Read ↗

Prenatal diagnosis of Apert syndrome.Semantic proximity Read ↗

Prenatal Diagnosis of Apert Syndrome due to A De novo FGFR2 Mutation at the Second Trimester: a case reportSemantic proximity Read ↗

Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants.Semantic proximity Read ↗

[Apert syndrome: clinico-epidemiological analysis of a series of consecutive cases in Spain].Semantic proximity Read ↗

Atypical presentation of a newborn with Apert syndrome.Semantic proximity Read ↗

Apert syndrome: evaluation of a treatment algorithm.Semantic proximity Read ↗

Early Prenatal Ultrasound and Molecular Diagnosis of Apert Syndrome: Case Report with Postmortem CT-Scan and Chondral Plate Histology.Semantic proximity Read ↗

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.Semantic proximity Read ↗

[Apert syndrome or acrocephalosyndactilia type I].Semantic proximity Read ↗

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