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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.[ncbi.nlm.nih.gov] Langer-Giedion syndrome , also known as trichorhinophalangeal syndrome type II, is an extremely rare autosomal dominant genetic disorder.[radiopaedia.org] 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[rarediseases.info.nih.gov]

  • Juvenile Rheumatoid Arthritis

    The disorder is characterized by microcephaly, growth retardation, immunodeficiency, and high incidence of cancer.[ncbi.nlm.nih.gov] JIA is a chronic disorder, which if neglected, can lead to serious complications.[en.wikipedia.org] D, Radiograph of the hands reveals joint space narrowing and erosions of the intercarpal joints, right worse than left.[med-ed.virginia.edu]

  • 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[ncbi.nlm.nih.gov] .: Surgical treatment of carpal tunnel syndrome and trigger digits in children with mucopolysaccharide storage disorders. J Hand Surg [Am] 23:236–243, 1998.[link.springer.com] Narrowing of the spinal canal ( spinal stenosis ) in the neck can compress and damage the spinal cord.[ghr.nlm.nih.gov]

  • 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[scielo.org.za] […] of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China.[ncbi.nlm.nih.gov] […] thoracic diameter, hand deformities, abnormal dentition).[orpha.net]

  • Familial Short Stature

    retardation.[ncbi.nlm.nih.gov] , Kozlowski type; brachyolmia; and familial digital arthropathy with brachydactyly [ 11 ]. 2.1.2.9.1.[intechopen.com] […] 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[aafp.org]

  • 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[ncbi.nlm.nih.gov] Abstract Coffin-Lowry syndrome (CLS) is an X-linked disorder characterized by facial dysmorphism, digit abnormalities and severe psychomotor retardation.[ncbi.nlm.nih.gov] A consistent feature is the large, puffy, soft hands with tapering fingers distally, small fingernails and full forearms.[genedx.com]

  • 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[ncbi.nlm.nih.gov] People with this inherited disorder have short stature and digits, facial distinctions including a broad skull and large tongue, and developmental delays.[khanacademy.org] […] and soles of feet Camptodactyly Slender body habitus and narrow pelvis Widely spaced nipples Trisomy 9 (usually mosaic) Mental retardation Intrauterine and postnatal growth[alpfmedical.info]

  • 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[researchgate.net] We report on a boy with prenatal growth retardation, progressive pancytopenia, cerebellar hypoplasia, microcephaly and developmental delay.[ncbi.nlm.nih.gov] […] 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[yumpu.com]

  • 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.[symptoma.com] Neonatal lymphedema, heart malformations, aplasia cutis congenita, aortic root dilatation, and autistic spectrum disorder have also been reported.[mendelian.co] The growth hormone insulin-like growth factor 1 axis in children and adolescents with inflammatory bowel disease and growth retardation.[scielo.br]

  • Kaufman Oculocerebrofacial Syndrome

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

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