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

Adams-Oliver syndrome: Additions to the clinical features and possible role of BMP pathway.

American journal of medical genetics. Part A - 1 Aug 2009

Baskar Shankar, Kulkarni Muralidhar Laxmanrao, Kulkarni Akhil Muralidhar, Vittalrao Suhasini, Kulkarni Preethi Muralidhar

Abstract excerpt

We report on a patient with Adams-Oliver syndrome, a condition characterized by scalp and limb defects. In addition we noted in our patient a significant delay in the bone age and an abnormal distal phalanx in one of her fingers manifesting clinically as a broad finger tip. Both these features hitherto unreported add to the phenotypic spectrum of the condition. The underlying etiopathogenesis of this condition...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Bone Morphogenetic Proteins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Infant

Share to Limb Deformities, Congenital

Share to Signal Transduction

Share to Syndrome

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 19606482
DOI: 10.1002/ajmg.a.32938

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Adams-Oliver syndrome: Additions to the clinical features and possible role of BMP pathway.PMID 19606482Read ↗

Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.Semantic proximity Read ↗

Adams-Oliver syndrome revisited.Semantic proximity Read ↗

Mutations in NOTCH1 cause Adams-Oliver syndrome.Semantic proximity Read ↗

Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.Semantic proximity Read ↗

Polymicrogyria associated with scalp and limb defects: Variant of Adams-Oliver syndromeSemantic proximity Read ↗

Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations.Semantic proximity Read ↗

Adams-Oliver syndrome: autosomal recessive inheritance and new phenotypic-anthropometric findings.Semantic proximity Read ↗

Possible common pathogenetic mechanisms for Poland sequence and Adams‐Oliver syndromeSemantic proximity Read ↗

Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.Semantic proximity Read ↗

Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams–Oliver syndromeSemantic proximity Read ↗

Severe phenotype in two half-sibs with Adams Oliver syndrome.Semantic proximity Read ↗

A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.Semantic proximity Read ↗

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