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440 Possible Causes for Disorder of Digit, Growth Retardation, Narrow Hands

  • Trichorhinophalangeal Syndrome

    The following is a case report of TRPSII with incomplete penetrance in the index case and exostoses and growth retardation in the patient's two siblings.[] Langer-Giedion syndrome , also known as trichorhinophalangeal syndrome type II, is an extremely rare autosomal dominant genetic disorder.[] Increased bone density of end part of the outermost hand bones 0010252 Microdontia Decreased width of tooth 0000691 Narrow palate Narrow roof of mouth 0000189 Osteoarthritis[]

  • Juvenile Rheumatoid Arthritis

    The disorder is characterized by microcephaly, growth retardation, immunodeficiency, and high incidence of cancer.[] JIA is a chronic disorder, which if neglected, can lead to serious complications.[] D, Radiograph of the hands reveals joint space narrowing and erosions of the intercarpal joints, right worse than left.[]

  • Mucopolysaccharidosis

    Previous reports on clinical characteristics of Morquio A mainly focused on growth retardation, skeletal deformities, and organ damage in children and adolescents, while the[] .: Surgical treatment of carpal tunnel syndrome and trigger digits in children with mucopolysaccharide storage disorders. J Hand Surg [Am] 23:236–243, 1998.[] Narrowing of the spinal canal ( spinal stenosis ) in the neck can compress and damage the spinal cord.[]

  • Cleidocranial Dysplasia

    Epiphysiodesis of the greater trochanter has only previously been described in association with mild cases of coxa vara, but we are considering early growth retardation of[] […] of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China.[] […] thoracic diameter, hand deformities, abnormal dentition).[]

  • Familial Short Stature

    retardation.[] , Kozlowski type; brachyolmia; and familial digital arthropathy with brachydactyly [ 11 ].[] […] the differential diagnosis of short stature. 5, 10, 11 The traditional method compares a plain radiograph of the left wrist and hand to a database of norms, although various[]

  • Coffin-Lowry Syndrome

    Abstract The Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation characterised in male patients by psychomotor and growth retardation, and various[] Abstract Coffin-Lowry syndrome (CLS) is an X-linked disorder characterized by facial dysmorphism, digit abnormalities and severe psychomotor retardation.[] A consistent feature is the large, puffy, soft hands with tapering fingers distally, small fingernails and full forearms.[]

  • Wolf-Hirschhorn Syndrome

    Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[] People with this inherited disorder have short stature and digits, facial distinctions including a broad skull and large tongue, and developmental delays.[] […] and soles of feet Camptodactyly Slender body habitus and narrow pelvis Widely spaced nipples Trisomy 9 (usually mosaic) Mental retardation Intrauterine and postnatal growth[]

  • Hoyeraal-Hreidarsson Syndrome

    Dermatologic evaluation revealed reticulated hyper- pigmentation on the neck, abdomen, extensor surfaces of the proximal phalanges of both hands and feet, wrists, palms, and[] We report on a boy with prenatal growth retardation, progressive pancytopenia, cerebellar hypoplasia, microcephaly and developmental delay.[] […] and 234: type 1 Keratodermia palmoplantaris Page 235 and 236: Landouzy-Dejerine muscular Pfeiffer Page 237 and 238: excavatum and rib and scapular anom Page 239 and 240: digital[]

  • Laron Syndrome with Immunodeficiency

    […] not observed either, if those with a short stature present dysmorphic features or evidence of skeletal dysplasia, or if growth retardation is severe.[] Neonatal lymphedema, heart malformations, aplasia cutis congenita, aortic root dilatation, and autistic spectrum disorder have also been reported.[] The growth hormone insulin-like growth factor 1 axis in children and adolescents with inflammatory bowel disease and growth retardation.[]

  • Kaufman Oculocerebrofacial Syndrome

    Proportionate growth retardation with a small head circumference/microcephaly, congenital malformations, muscular hypotonia, anomalies on brain imaging with hypoplasia of[] Fused eyelids, airway anomalies, ovarian cysts, and digital abnormalities in siblings: a new autosomal recessive syndrome or a variant of Fraser syndrome?[] , and long thin hands and feet.[]

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