Purpose: Chromosome 16p11.2 deletion syndrome (OMIM #611913) is a rare genetic condition resulting from the partial deletion of approximately 35 genes located at Chromosome 16. Affected people exhibit a variable clinical profile, featuring mild dysmorphisms, motor problems, developmental delay, mild intellectual disability (ID), socialization…

Stuttering places students at-risk for being stereotyped and experiencing identity difficulties in school. This study hoped to fill a lacuna in the literature on the educational experiences of African American male stutterers. Six African American adult males who stuttered and lived in Washington, DC; Maryland; and/or Virginia participated in this…

Although many children are referred with difficulties in both their speech and their language, the literature offers relatively little guidance on their therapy. Should clinicians treat these difficulties independently? Or should treatment depend on the potential impact of one domain on the other? This study aimed to investigate the relationship…

Aim: The aim of this study was to characterize the auditory brainstem responses (ABRs) of young children with suspected autism spectrum disorders (ASDs) and compare them with the ABRs of children with language delay and with clinical norms. Method: The ABRs of 26 children with suspected ASDs (21 males, five females; mean age 32.5 mo) and an age-…

The primary purpose of this study was to examine the influence of racial and ethnic backgrounds in children who stutter (CWS) with 18 specific coexisting disorders. A sample of 1,184 speech-language pathologists responded to a detailed questionnaire designed to answer questions about the type and prevalence of coexisting disorders in 2,535 CWS.…

Clause, syllable, and response latency characteristics of conversational utterances were assessed in 14 boys who stuttered and 14 normally fluent boys. Findings suggest that changes in the number of clausal constituents that must be constructed, stored, or coordinated within an utterance may influence the likelihood of speech errors and, hence,…

This study compared two methods of speech elicitation for phonological assessment: conversation and picture naming with 13 male phonologically impaired children (ages 4.2 to 5.11 years). Results suggest that both methods are useful clinical assessment tools but that the picture-naming test may tap the child's phonological system more deeply and be…

Forty-two children (29 boys and 13 girls), ages 3-10 years, were referred from the caseloads of clinical speech-language pathologists for suspected childhood apraxia of speech (CAS). According to results from tests of speech and oral motor skills, 22 children met criteria for CAS, including a severely limited consonant and vowel repertoire,…

Investigates the discourse coherence of school-aged children with Specific Language Impairment (SLI). Children with SLI were found to be significantly impaired in the areas of topic maintenance, event sequencing, explicitness, conjunctive cohesion, and fluency. Theoretical and clinical implications of the results are discussed. (Author/ER)

A study involving 51 speech-language pathologists serving 41 males (ages 2-9) with fragile X syndrome, found the majority reported the boys exhibit a visually based, experiential or holistic learning preference. Speech goals focused on slowing rate and increasing precision for verbal children and using assistive technology for nonverbal children.…