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

[Kabuki syndrome in the differential diagnosis of neonatal hypotonia].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Jan 2009

Aguilera Albesa S, Botella Astorqui M P, Ocio Ocio I

Abstract excerpt

No abstract is available from the source.

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 and Bones
Share to Diagnosis, Differential
Share to Face

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Intellectual Disability

Share to Muscle Hypotonia

Share to Phenotype

Source

Identifiers

PMID: 19174128
DOI: 10.1016/j.anpedi.2008.08.013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Kabuki syndrome in the differential diagnosis of neonatal hypotonia].PMID 19174128Read ↗

[The Kabuki syndrome].Semantic proximity Read ↗

[Clinical diagnosis of Kabuki syndrome: phenotype and associated abnormalities in two new cases].Semantic proximity Read ↗

Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literatureSemantic proximity Read ↗

Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype.Semantic proximity Read ↗

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSemantic proximity Read ↗

[Kabuki syndrome].Semantic proximity Read ↗

Extremely Low Birth Weight Infant (Gestational Age of 29 Weeks) With Kabuki Syndrome Type I: Case Report and Literature Review.Semantic proximity Read ↗

[Bartter syndrome, Gitelman syndrome, Liddle syndrome].Semantic proximity Read ↗

[Neonatal hypothyroidism].Semantic proximity Read ↗

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report.Semantic proximity Read ↗

[Clinical and molecular manifestations of congenital cerebral hypomyelination].Semantic proximity Read ↗

[Congenital syngnathia].Semantic proximity Read ↗

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