CC BY 4.0 · Arq Neuropsiquiatr 2024; 82(S 02): S53-S176
DOI: 10.1055/s-0045-1806971
ID: 541
Area: Others
Presentation method: Eletronic Poster

Neurodevelopmental delay characteristic of Pallister Killian syndrome

Laura França Malaquias
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Daniel Paulo Fonseca Dornelas
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
José Carlos Alves Neto
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Viviane Sandes de Barros
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Magno Martins Lobo
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Vanessa Loures Rossinol
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Ícaro Silva Magalhães
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
,
Fernanda de Carvalho Martins
1   Centro Universitário de Caratinga, Caratinga MG, Brazil.
2   Faculdade de Medicina do Vale do Aço, Ipatinga MG, Brazil.
› Author Affiliations
 

    *Correspondence: francalaura783@gmail.com.

    Abstract

    Case Presentation: An 8-year-old patient, male, non-verbal with delayed development in neuropsychomotor and language. The alterations were noticed at the age of 6 months, when the pediatrician who accompanied the case noticed the delay in development and referred him to the child neurologist, to the physiotherapist and to the speech therapist. The physiotherapy treatment provided normal gait and stability in gross movements, although, the fine movements didn’t develop. Even with the follow-up of speech therapy, the patient didn’t speak due to a maxillary monotony, emitting only babbling, despite his understanding not having any alterations, allowing the use of the Brazilian sign language for expression. Anatomical findings still culminate in sialorrhea, difficulty to sputum and dysphagia. The diagnosis was due to the karyotype test and the cytogenetic test, the arm count of the chromosomes identifies supernumerary short arms on chromosome 12.

    Discussion: The isochromosome 12 syndrome is a rare congenital anomaly, characterized by a mosaic chromosome 12 due to 2 extra numerals short arms. The principal symptoms presented are craniofacial dysmorphism, heart disease and delay in neurological development. Early detection of correlated symptoms as well as the follow-up with the multidisciplinary team improved the patient’s quality of life, which showed increased neurological development in the last years.

    Final Comments: Owing to the scarcity of available literature of chromosomal Pallister-Killian syndrome, this article aims to share information on the multidisciplinary follow-up of a case in Ipatinga-MG.


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    Publication History

    Article published online:
    12 May 2025

    © 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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