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336 Possible Causes for Mild to Moderate Short Stature

  • Aarskog-Scott Syndrome

    They frequently have mild to moderate short stature during childhood, but their growth usually catches up with that of their peers during puberty.[]

  • Schmid Metaphyseal Chondrodysplasia

    Type IV has an intermediate severity with a mild short stature, moderate deformities after recurrent fractures, dentinogenesis imperfecta and normal sclera.[] Type III has also a severe phenotype, but less than the type II, represented by very short stature, deformities, dentinogenesis imperfecta and blue sclera.[]

  • Osteogenesis Imperfecta Type 5

    OI type V is characterized by mild to moderate short stature, dislocation of the radial head, mineralized interosseous membranes, hyperplasic callus, white sclera and no dentinogenesis[] Clinical findings of OI type V include mild to moderate short stature, dislocation of the radial head, mineralized interosseous membranes, white sclera and no dentinogenesis[]

  • Growth Failure

    The main phenotypic features, reviewed by Leroy et al. [15], include mild-moderate developmental delay/intellectual disability, brachymetaphalangy of digits 3-5 (often digit[] 4 alone) ( 50%), short stature, obesity, hypotonia, characteristic facial appearance, autism or autism spectrum disorder (30%), joint hypermobility/dislocation, and scoliosis[]

  • Multiple Epiphyseal Dysplasia

    Multiple epiphyseal dysplasia (MED) is a common skeletal dysplasia characterized by mild to moderate short stature, early-onset of osteoarthritis (OA) mainly in the hip and[] short stature.[] The key features of MED are mild-to-moderate short stature and painful joints.[]

  • Osteogenesis Imperfecta

    Patients with type IV have moderately short stature, mild to moderate scoliosis, grayish or white sclera, and DI.[] Type V is characterized by mild to moderate short stature, dislocation of the radial head, mineralized interosseous membranes, hyperplastic callus, white sclera, and no DI[] Osteogenesis imperfecta type II is lethal, type III is severe, types IV and V are moderate, and type I is mild (see these terms).[]

  • Robinow Syndrome

    From Wikidata Jump to navigation Jump to search syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities[] […] to moderate short stature (dwarfism) - Short lower arms (mesomelic brachymelia - Small hands with clindodactyly and brachymesophalangy or achydactyly - of fifth finger (short[] OI type IV - moderately severe form Characteristics include the following: Mild to moderate bone deformity Variable short stature Hearing loss occurs in some families Variable[]

  • Epilepsy

    ID mild ID mild to moderate ID, speech impairment severe ID mild ID moderate to severe ID unspecified delay Other clinical findings ataxia, relative microcephaly, mild facial[] […] dysmorphisms microcephaly, short stature, mild facial dysmorphisms microcephaly, congenital hypothyroidism, bicuspid aortic valve, hypotonia microcephaly, short stature,[] Development prior to epilepsy not specified delayed delayed delayed delayed delayed normal or delayed normal Developmental outcome globally delayed, severe speech impairment mild[]

  • Kabuki Syndrome

    […] and short stature.[] […] to moderate intellectual delay short stature abnormalities of the skeleton / joint laxity / hypotonia/loose joints unusual skin ridge patterns on the fingers, toes, palms[] Intellectual disability (mild to moderate). Postnatal short stature What's the Co-Existing Problem? Kabuki is a complex syndrome with many associated findings.[]

  • Eye Muscle Disorder

    […] to moderate intellectual disability; and short stature.[] […] eyebrows with sparseness in the outer half, misshapen or prominent ears, depressed nasal tip; skeletal abnormalities of the fingers or vertebrae; persistent finger fetal pads, mild[]

Further symptoms