Create issue ticket

1,445 Possible Causes for Mild Developmental Delay

  • Ring Chromosome 19

    We report on a 5-year-old girl with mild developmental delay and dysmorphic features which were previously unrecognized.[ncbi.nlm.nih.gov] developmental delay due to ring chromosome 19 mosaicism. ( 10068050 ) Vaz I....Green S.H. 1999 5 Mosaic supernumerary ring chromosome 19 identified by comparative genomic[malacards.org] Vaz I, Larkins SA, Norman A, Green SH: Mild developmental delay due to ring chromosome 19 mosaicism. Dev Med Child Neurol 41:48–50 (1999).[karger.com]

  • Subcortical Band Heterotopia

    Although he had infantile spasms from 5-months old and showed mild developmental delay, he responded well to vitamin B6 and ACTH therapy.[ci.nii.ac.jp] The SBH patients had mild to moderate developmental delays, drug-resistant generalized seizures, and diffuse thick SBH upon brain MRI.[ncbi.nlm.nih.gov]

  • Vitamin B12 Deficiency

    […] hypotonia and mildly enlarged liver and spleen Persistence of mild hypotonia Persistence of mild hypotonia Pathological neurological findings Significant delay in developmental[doi.org] […] feeding difficulties, severe pallor, muscle hypotonia, somnolence, enlarged liver and spleen Persistence of hypotonia and mildly enlarged liver and spleen Persistence of mild[doi.org]

  • Glutamate Formiminotransferase Deficiency

    Features of a mild phenotype include high urinary excretion of FIGLU in the absence of histidine administration, mild developmental delay, and no hematological abnormalities[ncbi.nlm.nih.gov] developmental delay and elevated concentrations of formiminoglutamate (FIGLU) in the urine.[orpha.net] […] disease Formiminoglutamic aciduria Disease definition Formiminoglutamic aciduria, in its moderate form and in the absence of histidine administration, is characterized by mild[orpha.net]

  • Hypogonadism

    delay, and mild cognitive impairments.[ncbi.nlm.nih.gov] Here, we describe a 2-year-5-month-old boy with severe congenital heart defects, limb anomalies, hypogonadism, distinctive facial features, pre- and postnatal developmental[ncbi.nlm.nih.gov]

  • Growth Failure

    developmental delay.[karger.com] Neurological evaluation revealed mild developmental delay (he had a developmental age of 15 months at the age of 2 years in according to Griffith scale) and global hypotonia[cyberleninka.org] A case of partial IGF-I deficiency has also been described and was associated with pre- and postnatal growth retardation and microcephaly but the developmental delay was mild[orpha.net]

  • Puerperium

    Children with a history of NE who suffer from CP at the age of 12 months are often also severely developmentally delayed.[doi.org] Of the children without CP, those with mild NE have an excellent prognosis.[doi.org]

  • Birth

    Children with a history of NE who suffer from CP at the age of 12 months are often also severely developmentally delayed.[doi.org] Of the children without CP, those with mild NE have an excellent prognosis.[doi.org]

  • Fetal Hydantoin Syndrome

    developmental delays.[rarediseases.info.nih.gov] However, characteristic features may include distinctive skull and facial features, growth deficiencies, underdeveloped (hypoplastic) nails of the fingers and toes, and/or mild[rarediseases.org] Symptoms in affected individuals may include abnormalities of the skull and facial features, growth deficiencies, underdeveloped nails of the fingers and toes, and/or mild[rarediseases.info.nih.gov]

  • Autosomal Recessive Spastic Paraplegia Type 20

    SPG20 is characterized by dysarthria, distal amyotrophy, mild developmental delay and short stature. {ECO:0000269 PubMed:12134148}.[genecards.org] SPG20 is characterized by dysarthria, distal amyotrophy, mild developmental delay and short stature.[mybiosource.com]

Further symptoms