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198 Possible Causes for Short Stature in First Year of Life

  • Cystitis

    Affected individuals typically have normal early development in the first year or so of life, followed by development regression and the development of symptoms.[ncbi.nlm.nih.gov] year of life, whereas retinal dystrophy had a more variable age of onset.[ncbi.nlm.nih.gov] There was severe disproportionate short stature, with a final height of less than 100 cm; scoliosis was usually mild.[ncbi.nlm.nih.gov]

  • Nephropathic Cystinosis

    Abstract In long-standing nephropathic cystinosis complications are observed in various organs. Distal myopathy was first described in detail in 1994. The prevalence was calculated to be 24%. We studied seven patients with nephropathic cystinosis with neurophysiological techniques. Only two patients complained of a[…][ncbi.nlm.nih.gov]

  • Cystocele

    Affected individuals typically have normal early development in the first year or so of life, followed by development regression and the development of symptoms.[ncbi.nlm.nih.gov] year of life, whereas retinal dystrophy had a more variable age of onset.[ncbi.nlm.nih.gov] There was severe disproportionate short stature, with a final height of less than 100 cm; scoliosis was usually mild.[ncbi.nlm.nih.gov]

  • Tumor Lysis Syndrome

    Children may initially display normal growth, usually for the first few years of life.[rarediseases.org] Almost all females with Turner syndrome exhibit growth failure and attain a final height that is shorter than average (short stature).[rarediseases.org]

  • Coxa Vara

    Affected individuals typically have normal early development in the first year or so of life, followed by development regression and the development of symptoms.[ncbi.nlm.nih.gov] year of life, whereas retinal dystrophy had a more variable age of onset.[ncbi.nlm.nih.gov] There was severe disproportionate short stature, with a final height of less than 100 cm; scoliosis was usually mild.[ncbi.nlm.nih.gov]

  • Familial Infantile Myoclonic Epilepsy

    Symptomatic generalized epilepsies Infantile spasms Mostly within the first year of life (peak 4-6 months) and cease by 5 years of age West syndrome Triad: infantile spasms[emilytam.com] stature Pathological features: Ragged-red fibers Lesions of dentate and inferior olives Degeneration of cerebellum, brainstem, and spinal cord Astrocytosis, demyelination[emilytam.com] […] myoclonic epilepsy, GTC seizures, ataxia, action-induced polymyoclonus Late – progressive muscle weakness, hypertrophic cardiomyopathy, dementia, deafness, multiple lipomata, short[emilytam.com]

  • Benign Familial Infantile Epilepsy Type 4

    Symptomatic generalized epilepsies Infantile spasms Mostly within the first year of life (peak 4-6 months) and cease by 5 years of age West syndrome Triad: infantile spasms[emilytam.com] stature Pathological features: Ragged-red fibers Lesions of dentate and inferior olives Degeneration of cerebellum, brainstem, and spinal cord Astrocytosis, demyelination[emilytam.com] […] myoclonic epilepsy, GTC seizures, ataxia, action-induced polymyoclonus Late – progressive muscle weakness, hypertrophic cardiomyopathy, dementia, deafness, multiple lipomata, short[emilytam.com]

  • Growth Hormone Deficiency

    Knowing the growth patterns of these entities in the first years of life might be helpful to distinguish them from growth hormone deficiency (GHD) or other chronic diseases[ncbi.nlm.nih.gov] BACKGROUND: Familial short stature (FSS) and constitutional delay of growth (CDG) are the most frequent norm variants in children presenting with short stature.[ncbi.nlm.nih.gov]

  • Coxa Valga

    Major findings are likely to be present in the first year of life.[ncbi.nlm.nih.gov] stature, short hands and feet, progressive joint limitation and contractures, distinctive facial features, progressive cardiac valvular disease, and thickened skin.[ncbi.nlm.nih.gov] MedGen UID: 479777 • Concept ID: C3278147 • Disease or Syndrome Geleophysic dysplasia, a progressive condition resembling a lysosomal storage disorder, is characterized by short[ncbi.nlm.nih.gov]

  • Panayiotopoulos Syndrome

    Symptomatic generalized epilepsies Infantile spasms Mostly within the first year of life (peak 4-6 months) and cease by 5 years of age West syndrome Triad: infantile spasms[emilytam.com] stature Pathological features: Ragged-red fibers Lesions of dentate and inferior olives Degeneration of cerebellum, brainstem, and spinal cord Astrocytosis, demyelination[emilytam.com] […] myoclonic epilepsy, GTC seizures, ataxia, action-induced polymyoclonus Late – progressive muscle weakness, hypertrophic cardiomyopathy, dementia, deafness, multiple lipomata, short[emilytam.com]

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