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67 Possible Causes for Failure to Thrive, Progressive Action Tremor

  • Cockayne Syndrome

    […] dysmetria and action tremor observed in patients with CS.[ajnr.org] Of these, failure to thrive, photosensitivity, and intellectual disability (language delays) developed before 2 or 3 years of age, whereas deafness, sunken eyes, and basal[ncbi.nlm.nih.gov] CAMFAK syndrome is an inherited disease characterized by congenital cataracts, microcephaly, failure to thrive, and kyphoscoliosis with onset in early infancy.[ncbi.nlm.nih.gov]

  • Mental Retardation

    One of several phenotypes associated with different mutations of the fragile X mental retardation 1 gene (FMR1), FXTAS involves progressive action tremor, gait ataxia, and[ncbi.nlm.nih.gov] The patient presented with exocrine pancreatic insufficiency as well as failure-to-thrive.[ncbi.nlm.nih.gov] Translated by Apolline Morville B.2 Failure to thrive or weight faltering in a primary health care setting (824 KB PDF) Astrid Berg VERSION IN FRENCH: “ Retard de croissance[web.archive.org]

  • Olivopontocerebellar Atrophy

    Tremor - Postural, resting, or both Bradykinesia plus at least 1 parkinsonian feature Cerebellar Dysfunction • Gait ataxia (wide-based stance with steps of irregular length[physio-pedia.com] The clinical features (failure to thrive, hypotonia, liver disease, effusions, and visual inattention) were similar to those of the four cases already reported, as were the[ncbi.nlm.nih.gov] The clinical and pathologic features of 2 brothers who presented in early infancy with failure to thrive and neurologic deterioration leading to death by the age of 5 months[ncbi.nlm.nih.gov]

  • Cerebral Palsy

    The most common manifestation of ataxic cerebral palsy is intention (action) tremor, which is especially apparent when carrying out precise movements, such as tying shoe laces[en.wikipedia.org] The individual had a history of failure to thrive, bowel and bladder incontinence, reduced bone mineral density (BMD) for age, and spinal deformity at the time exercise was[ncbi.nlm.nih.gov] Gastrointestinal symptoms and their sequelae - eg, reflux, oropharyngeal muscle disorders, failure to thrive and osteoporosis.[patient.info]

  • Short stature-Valvular Heart Disease-Characteristic Facies Syndrome

    Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant disorder characterized by action tremor of the upper extremities progressing to ataxia and other cerebellar[chginc.org] He had persistent failure to thrive due to intermittent respiratory tract infection.[indianjotol.org] Slow weight gain, especially during the first several years of life, is also a common problem and many children are diagnosed as "failure to thrive".[williams-syndrome.org]

  • Tay-Sachs Disease

    […] syndrome, along with irregular action tremor and stimulus-sensitive myoclonus of the arms.[ncbi.nlm.nih.gov] This report describes a case report of a postmortem performed on a 5-year old patient of Tay-Sachs disease, presenting with failure to thrive, muscular flaccidity, and cherry-red[ncbi.nlm.nih.gov] We discuss the assessment and differential diagnoses of a young adult Hungarian man with a 1-year history of a progressive and symmetric amyotrophic lateral sclerosis-like[ncbi.nlm.nih.gov]

  • Neurodegenerative Disorder

    tremor, myoclonus, hyper-reflexia, and focal limb dystonia.[aao.org] Characteristic presentations are failure to thrive, cerebellar ataxia, respiratory insufficiency, and hypotonia or hypertonia.[ncbi.nlm.nih.gov] Main features of agenesis of corpus callosum (ACC), hypopigmentation, immunodeficiency/recurrent infections, cataracts, severe failure to thrive, and profound psychomotor[ncbi.nlm.nih.gov]

  • X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome

    Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant disorder characterized by action tremor of the upper extremities progressing to ataxia and other cerebellar[chginc.org] […] to thrive Gait ataxia Ataxia Hypertelorism Neonatal hypotonia Rare Symptoms - Less than 30% cases Autosomal recessive inheritance Motor delay Myopathy Nystagmus Long philtrum[mendelian.co] The other important features include- seizures, failure to thrive, scoliosis and osteopenia.[iamg.in]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant disorder characterized by action tremor of the upper extremities progressing to ataxia and other cerebellar[chginc.org] […] to thrive / difficulties for feeding in infancy / growth delay - Hypotonia - Intellectual deficit / mental / psychomotor retardation / learning disability - Kyphosis - Long[csbg.cnb.csic.es] Gastroenterologic • Considerations: • failure to thrive (35%) • Dysphagia – poor coordination of swallow and airway closure • Chewing difficulties – masticatory and facial[slideshare.net]

  • Spinocerebellar Ataxia Type 12

    SCA12 is a late-onset, autosomal dominant, slowly progressive disorder. Action tremor is the usual presenting sign.[jhu.pure.elsevier.com] Clinical features Stage of ataxia; mental deficiency during infantile and childhood stage Delayed development, failure to thrive, hypotonia, and multisystem organ failure[emedicine.medscape.com] SCA12 is a late-onset, autosomal dominant , slowly progressive disorder. Action tremor is the usual presenting sign.[ncbi.nlm.nih.gov]

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