Purpose: In this article, the authors address the hypothesis that the severe and persistent speech disorder reported in persons with galactosemia meets contemporary diagnostic criteria for Childhood Apraxia of Speech (CAS). A positive finding for CAS in this rare metabolic disorder has the potential to impact treatment of persons with galactosemia…

Purpose: The aims of this study were (a) to locate the breakpoints of a balanced translocation (7;13) within a mother (B) and daughter (T); (b) to describe the language and cognitive skills of B and T; and (c) to compare this profile with affected family members of the KE family who have a mutation within "FOXP2." Method: The breakpoint locations…

Purpose: In this study, the authors evaluated literacy outcome in children with histories of speech sound disorder (SSD) who were characterized along 2 dimensions: broader language function and persistence of SSD. In previous studies, authors have demonstrated that each dimension relates to literacy but have not disentangled their effects.…

Purpose: Conceptual and methodological confounds occur when non(sense) word repetition tasks are administered to speakers who do not have the target speech sounds in their phonetic inventories or who habitually misarticulate targeted speech sounds. In this article, the authors (a) describe a nonword repetition task, the Syllable Repetition Task…

Purpose: The primary goal of this case study was to describe the speech, prosody, and voice characteristics of a mother and daughter with a breakpoint in a balanced 7;13 chromosomal translocation that disrupted the transcription gene, "FOXP2" (cf. J. B. Tomblin et al., 2005). As with affected members of the widely cited KE family, whose…

This report presents findings supporting the hypothesis of a clinically relevant subtype of childhood speech sound disorder, provisionally titled speech delay--developmental psychosocial involvement (SD-DPI). Conversational speech samples from 29 children who met inclusionary criteria for SD-DPI were selected from a case record archive at a…

Converging evidence supports the hypothesis that the most common subtype of childhood speech sound disorder (SSD) of currently unknown origin is genetically transmitted. We report the first findings toward a set of diagnostic markers to differentiate this proposed etiological subtype (provisionally termed "speech delay-genetic") from other…

This study compared the speech and prosody-voice profiles for 30 male speakers with either high-functioning autism (HFA) or Asperger syndrome (AS), and 53 typically developing male speakers. Both HFA and AS groups had more residual articulation distortion errors and utterances coded as inappropriate for phrasing, stress, and resonance. AS speakers…

A study of 35 3-year-olds followed since infancy in a university-affiliated pediatrics clinic and 50 Native American children followed since infancy in a tribal health clinic found early recurrent otitis media with effusion was only associated with increased risk for speech disorder in the Native American children. (Contains extensive references.)…

A study of 70 children found that hearing levels at 12-18 months were significantly associated with speech delay and low language outcomes at 3 years of age. Significant and substantial effects of hearing levels at 12-18 months on speech status at 3 years were significantly mediated by language status at 3 years. (Contains extensive references.)…

This study attempted to identify diagnostic markers for suspected developmental apraxia of speech (SD-DAS) in 30 children with either SD-DAS or speech delay using analytic procedures from metrical phonology. Findings indicated that, although lexical metrical patterns did not differentiate the groups, syllable omissions persisted until much later…

This study estimated the incidence of speech delay based on a demographically representative sub-sample of 1,328 monolingual English-speaking 6-year-old children. Among six major findings were: (1) the prevalence of speech delay was 3.8 percent; (2) speech delay was 1.5 times more prevalent in boys than girls; and (3) comorbidity of speech delay…

Discusses developmental apraxia of speech (DAS), a putative diagnostic category for children whose speech errors differ from errors of children with developmental speech delay and resemble errors of adults with acquired apraxia of speech. A study of 148 children with language impairments investigated the diagnosis of DAS. (Author/CR)

Discusses a study that compared speech and prosody-voice profiles of children (ages 4-14) with suspected developmental apraxia of speech (DAS) to profiles of 73 children with speech delay. Also describes a second study of 20 children (ages 3-9) that investigated whether stress was a diagnostic marker of DAS. (Author/CR)

A study used the conversational speech samples from 19 children (ages 4-14) with suspected developmental apraxia of speech (DAS) to investigate the characteristics of the disability. The results of the study, combined with the results of two previous studies, indicate inappropriate stress is a diagnostic marker for DAS. (Author/CR)