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

[Rett phenotype in patient with XXY karyotype: case report].

Arquivos de neuro-psiquiatria - 1 Dec 1998

Schwartzman J S, De Souza A M, Faiwichow G, Hercowitz L H

Abstract excerpt

We report the case of a XXY boy who presents progressive neurological disorder which has started around eleven months of age, with developmental stagnation followed by regression. The child presents as well stereotypic hand movements, loss of purposeful hands use and microcephalia. Presence of any defined systemic or neurological condition which could be pointed out as the possible etiological factor for the case...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Karyotyping
Share to Klinefelter Syndrome

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

Share to Phenotype

Share to Rett Syndrome

Source

Identifiers

PMID: 10029889
DOI: 10.1590/s0004-282x1998000500020

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

[Rett phenotype in patient with XXY karyotype: case report].PMID 10029889Read ↗

[Developmental disorder in girls due to Rett syndrome].Semantic proximity Read ↗

Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).Semantic proximity Read ↗

[Tetra-X syndrome with epilepsy, mental retardation and multiple dysmorphias].Semantic proximity Read ↗

[Genetic basis for Rett disease].Semantic proximity Read ↗

[49 XXXXY syndrome. Description of 2 clinical cases].Semantic proximity Read ↗

[Rett syndrome--case report].Semantic proximity Read ↗

[Rett syndrome in a child treated with adrenocorticotrophic hormone].Semantic proximity Read ↗

Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.Semantic proximity Read ↗

[Speech and motor disorders in Rett syndrome].Semantic proximity Read ↗

[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations].Semantic proximity Read ↗

[Behavioral and neuropsychological phenotype of the 48XXYY syndrome: a longitudinal study of a case].Semantic proximity Read ↗

[46 XX karyotype men (author's transl)].Semantic proximity Read ↗

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