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677 Possible Causes for Moderately Short Stature

  • Growth Failure

    4 alone) ( 50%), short stature, obesity, hypotonia, characteristic facial appearance, autism or autism spectrum disorder (30%), joint hypermobility/dislocation, and scoliosis[cyberleninka.org] Other indications GH responses in other short stature syndromes, such as Down’s, and Noonan syndromes, have all shown similar responses to those observed with Turner syndrome[pharmaceutical-journal.com] The main phenotypic features, reviewed by Leroy et al. [15], include mild-moderate developmental delay/intellectual disability, brachymetaphalangy of digits 3-5 (often digit[cyberleninka.org]

  • Cleidocranial Dysplasia

    short stature, delayed eruption of permanent dentition and supernumerary teeth.[ncbi.nlm.nih.gov] short stature Moderate short stature 0008848 Neonatal respiratory distress Infantile respiratory distress Newborn respiratory distress Respiratory distress, neonatal [ more[rarediseases.info.nih.gov] Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in[dentalimplants-usa.com]

  • Aarskog-Scott Syndrome

    A growth spurt in late teens, generally, results in a moderate short stature.[orpha.net] They frequently have mild to moderate short stature during childhood, but their growth usually catches up with that of their peers during puberty.[en.wikipedia.org] Size is generally normal at birth, but growth is slow in infancy and childhood, leading to short stature until puberty, which is often delayed.[orpha.net]

  • 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[wikidata.org] short stature.[ncbi.nlm.nih.gov] short stature (dwarfism) - Short lower arms (mesomelic brachymelia - Small hands with clindodactyly and brachymesophalangy or achydactyly - of fifth finger (short fingers[ibis-birthdefects.org]

  • Baraitser-Winter Syndrome 1

    Other features include moderate short stature, contractures, congenital cardiac disease and genitourinary malformations.[doi.org] Other features include moderate short stature… CONTINUE READING[semanticscholar.org]

  • Acne Vulgaris

    […] hirsutism, menstrual irregularity / fertility problems and a short stature There is often a family history Patients normally have biochemical evidence of hyperandrogenism[pcds.org.uk] […] features: Clinical features in childhood include precocious puberty, acne and accelerated bone age Clinical features in adolescent and adult females include persistent acne, moderate-severe[pcds.org.uk]

  • 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[orpha.net] 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[iofbonehealth.org]

  • Osteogenesis Imperfecta

    Patients with type IV have moderately short stature, mild to moderate scoliosis, grayish or white sclera, and DI.[orpha.net] 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[orpha.net] The main signs of type III include very short stature, a triangular face, severe scoliosis, grayish sclera, and DI.[orpha.net]

  • 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[ncbi.nlm.nih.gov] short stature.[ncbi.nlm.nih.gov] Clinical description EDM1 (see this term) is clinically the best characterized form of EMD and is marked by a waddling gait and pain at onset, and moderate short stature.[orpha.net]

  • Autosomal-Recessive Robinow Syndrome

    Typical features of these conditions include mild to moderate short stature, distinctive facial features, skeletal abnormalities, and abnormal development of the genitalia[encyclopedia.com] Most children with Robinow syndrome experience growth delays after birth, resulting in slight to moderate short stature.[rarediseases.org]

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