Özet:

Introduction: Partial trisomy 8q and 21p cooccurrences are quite rare structural chromosomal disorders. Partial 8q duplications usually include mental retardation, hypertelorism, a flattened nasal root and cleft palate. This study, aimed presents findings on the speech and language evaluation of a 5 year 7 months-old male with a previously reported maternal transitional trisomy 8q and monosomy 21p. The article presents the child’s mental, developmental, language, speech, behavioral and psychological features and explains possible strategies of speech and language intervention. Method: In the evaluation of the subject, Ankara Developmental Screening Inventory (AGTE), Developmental Screening Test (Denver II), Turkish Articulation and Phonology Test (SST), Kay PENTAX Nasometer II, Turkish version of Test of Early Language Development (TELD-3) (TEDIL), SALT Windows Clinical V9 (Turkish) and audiological evaluation standard techniques were used. In addition, oral-motor evaluation and language sample analysis were informally performed. Results and discussion: All of the standardized and informal assessment tools used revealed that the subject had significant impairments in all areas of development, in oral structure and function and in all components of language and speech and behavior. Oral evaluation showed that the child had repaired bilateral complete cleft, 2-5 mm fistula at the incisive foramen and a bifid uvula, limited movement of the velum which explained the nasality (Table 1). The child could chew, swallow and had no drooling. According to Denver II Developmental Screening Test-Turkish (Yalaz, Anlar ve Bayoğlu, 2010), the subject showed delay in all areas of development except for fine motor skills. Ankara Developmental Inventory (Savaşır, Sezgin ve Erol, 1998), however, revealed delay in all areas of development, ranging from 22-23 months in gross motor skills to 3 years 3-5 months in social skills and language. Based on the spontaneous conversation sample taken, the subject was found to have, in his phonetic inventory, /b, d, h, m, ʋ, j/ sounds in initial position, /b, m, n, ʋ, j/ in medial position and /l, s, t, j/ in final position. On the picture-naming subtest of The Articulation and Phonology Test (SST) (Topbaş, 2005), the subject had an age equivalent of <2.0 and on the auditory discrimination subtest, an age equivalent of >3, which indicated that sound discrimination was not the reason for his articulatory and/or phonological problems. The subject was found to use a number of phonological processes which included metathesis in word-final position which included /s, z, ʤ, ʧ, ʒ/ sounds, syllable deletion, de-nasalization, fronting, devoicing and gliding. The subject was observed to be over-active, had trouble establishing joint attention, had low intelligibility, and trouble starting and maintaining conversation. Based on TEDİL, the Turkish Early Language Development Test (Topbaş and Güven, 2011), his receptive language age was 3 years 3 months and expressive age, 4.0 years. His MLU was found to be 1.02, which, according to Turkish norms (Ege, Acarlar and Güleryüz, 1998), has an ageequivalent of 18.59 months. He was occasionally observed to use only the past tense suffixes -dı (definite) and mIs (story), the present continuous -Iyor and the dative -e and the accusative -I as well as the possessive -m. Therapy with this case took place one a week for 8 weeks and was based on evidence based naturalistic techniques. The aims included awareness of articulation positions, producing bilabial /p, b/ and alveolar /t, d/ sounds, teaching the negative suffix and others. The family was also advised about how to increase his vocabulary. In this case-study, the subject with the partial trisomy 8q and 21p co-occurrence was found to have not only a developmental delay but also varying degrees of delays in all components of language. Particularly, his intelligibility was found to be more related to his phonological problems than his cleft palate. Also, most important issues of speech and language disorders related to craniofacial anomalies and the subsequent therapies are here discussed in light of the relevant literature

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