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14 Possible Causes for Speech Delay (59%)

Did you mean: Speech Delay (59, )

  • Autistic Disorder

    ) Motor delay 9–19% Physical therapy Hypotonia 50% Physical therapy Psychiatric 22 Anxiety 43–84% Behavioural treatment such as relaxation, cognitive behavioural treatment[ncbi.nlm.nih.gov] […] and language therapy Attentional problems, impulsivity, or hyperactivity 59% Behavioural intervention, psychopharmacotherapy (eg, stimulants, atomoxetine, or alpha blockers[ncbi.nlm.nih.gov] Comorbid symptoms or disorders Frequency Treatments Developmental 5 Cognitive; intellectual disability 40–80% Educational Language deficits 50–63% Communication training, speech[ncbi.nlm.nih.gov]

  • Cornelia De Lange Syndrome

    ) feeding difficulties (chewing & swallowing problems, regurgitation, projectile vomiting) developmental delay/MR (moderate to severe, usually) - IQ range 30-86 (ave. 53)[en.wikibooks.org] […] significant speech/communication delay and psychomotor delay behavioral problems (acting out) limb abnormalities (reduction defects - missing forelimbs or portions thereof[en.wikibooks.org] […] bicornate uterus) hypoplasia of male genitalia with undescended testes or hypospadias seizures (11-23%) congenital heart defects (20-25%) cleft palate or high arched palate (18-59%[en.wikibooks.org]

  • Adenosine Deaminase Deficiency

    Neurological symptoms were found in 59%(54), and categorized as ocular dysfunction(32), appendicular motor or sensory dysfunction(25), coordination disturbances(16), speech[neurology.org] […] difficulty(12), altered mental status(12), headache(10), developmental delay(4), seizure(3), or other(15).[neurology.org]

  • Bardet-Biedl Syndrome Type 11

    Speech deficit Speech delay/deficit, requiring speech therapy, was reported in 59 patients (54%).[jmg.bmj.com]

  • 8p Inverted Duplication / Deletion Syndrome

    32 hallmark (90%) Very frequent (99-80%) HP:0000400 9 wide nasal bridge 59 32 frequent (33%) Frequent (79-30%) HP:0000431 10 delayed speech and language development 59 32[malacards.org] Occasional (29-5%) HP:0000826 6 seizures 59 32 occasional (7.5%) Occasional (29-5%) HP:0001250 7 scoliosis 59 32 occasional (7.5%) Occasional (29-5%) HP:0002650 8 macrotia 59[malacards.org]

  • Smith-Magenis Syndrome

    delay, hoarse deep voice and peripheral neuropathy.[ncbi.nlm.nih.gov] […] features of this syndrome which is also referred to as the Smith-Magenis syndrome consist of a broad flat midface with brachycephaly, broad nasal bridge, brachydactyly, speech[ncbi.nlm.nih.gov] The remarkable consistency of the main clinical features of the 59 patients documented so far permits the clinical diagnosis of this syndrome; a fact which is of importance[ncbi.nlm.nih.gov]

  • Hyperextensible Joints

    Developmental concerns were not limited to the motor systems however, and 59% were recorded to have had speech delay and 39% had some degree of ‘mental retardation’.[docksci.com]

  • Eyebrow Duplication - Syndactyly Syndrome

    ) feeding difficulties (chewing & swallowing problems, regurgitation, projectile vomiting) developmental delay/MR (moderate to severe, usually) - IQ range 30-86 (ave. 53)[en.wikibooks.org] […] significant speech/communication delay and psychomotor delay behavioral problems (acting out) limb abnormalities (reduction defects - missing forelimbs or portions thereof[en.wikibooks.org] […] bicornate uterus) hypoplasia of male genitalia with undescended testes or hypospadias seizures (11-23%) congenital heart defects (20-25%) cleft palate or high arched palate (18-59%[en.wikibooks.org]

  • Bardet-Biedl Syndrome 10

    Renal anomalies 53% Learning difficulties 61% Secondary features Speech delay 54–81% Developmental delay 50–91% Diabetes mellitus 6–48% Dental anomalies 51% Congenital heart[de.slideshare.net] Frequency Primary features Rod-cone dystrophy 93% Polydactyly 63–81% All four limbs: 21% Upper limbs only: 9% Lower limbs only:21% Obesity 72–92% Genital anomalies 59–98%[de.slideshare.net]

  • Nonsyndromic Renal Hypodysplasia Type 1

    300630 ) Description: X-linked ID and autism syndrome characterized by hypotonia, speech delay, aggressive behavior, and brain calcifications.[autismkb.cbi.pku.edu.cn] Reference(s): 20159109 ; AutG8905 AP1S2 Xp22.2 adaptor-related protein complex 1, sigma 2 subunit XL X-linked mental retardation syndromeMental retardation, X-linked 59 ([autismkb.cbi.pku.edu.cn]

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