The role of multidisciplinary diagnostic and therapeutic model of care in Lamb-Shaffer syndrome - case report

© 2024. The Author(s)..

This case study illustrates a multidisciplinary diagnostic and therapeutic model of care for a 7-year-old male with Lamb-Shaffer syndrome (LAMSHF). LAMSHF is an ultra-rare genetic neurodevelopmental disorder, caused by heterozygous alterations in the SOX5 gene. An integrative model of therapy of cognitive functions and speech is described. The presented approach allows the development of language competences through stimulation of basic cognitive functions, which allows the learning of the abstract rules of an inflected language. A surprising, unexpected improvement in the cognitive functioning of the child was observed (both in terms of reasoning and speech), as well as an increase in his independence. The clinically important problem of the need for continued stimulation of cognitive development, in spite of the unfavourable prognosis associated with LAMSHF, is highlighted.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - year:2024

Enthalten in:

Journal of applied genetics - (2024) vom: 10. Feb.

Sprache:

Englisch

Beteiligte Personen:

Sajewicz-Radtke, Urszula [VerfasserIn]
Łada-Maśko, Ariadna [VerfasserIn]
Lipowska, Małgorzata [VerfasserIn]
Radtke, Bartosz M [VerfasserIn]
Lipska-Ziętkiewicz, Beata S [VerfasserIn]
Krempla-Patron, Katarzyna [VerfasserIn]

Links:

Volltext

Themen:

Intelligence
Journal Article
LAMSHF
Language
Primary school
Rare genetic diseases

Anmerkungen:

Date Revised 10.02.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.1007/s13353-024-00838-3

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM368298000