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211 Possible Causes for Diffuse Osseous Demineralization, Mild Blepharophimosis

  • Warburg Micro Syndrome 3

    Radiological examination of the skeleton showed a left curved scoliosis, convex vertebral bodies, diffuse osseous demineralization, thin diaphyses of the long bones, bilateral[cags.org.ae]

  • Benign Adult Familial Myoclonic Epilepsy

    […] syndactyly) (Saethre-Chotzen syndrome with eyelid anomalies, included) (Blepharophimosis, epicanthus inversus, and ptosis 3, formerly; BPES3, included) 14 101600 Pfeiffer[becomerich.lab.u-ryukyu.ac.jp] […] cephalodactyly, included) 13 101400 Saethre-Chotzen syndrome (SCS) (Acrocephalosyndactyly, type III; ACS3) (ACS III) (Chotzen syndrome) (Acrocephaly, skull asymmetry and mild[becomerich.lab.u-ryukyu.ac.jp]

    Missing: Diffuse Osseous Demineralization
  • Lyme Disease

    osseous structures.[doi.org] The one patient in the doxycycline group who reported severe arthralgia at the last follow-up had a history of multiple dorsal and lumbar fractures with diffusely demineralized[doi.org]

    Missing: Mild Blepharophimosis
  • Lyme Neuroborreliosis

    osseous structures.[doi.org] The one patient in the doxycycline group who reported severe arthralgia at the last follow-up had a history of multiple dorsal and lumbar fractures with diffusely demineralized[doi.org]

    Missing: Mild Blepharophimosis
  • Early Infantile Epileptic Encephalopathy Type 2

    […] syndactyly) (Saethre-Chotzen syndrome with eyelid anomalies, included) (Blepharophimosis, epicanthus inversus, and ptosis 3, formerly; BPES3, included) 14 101600 Pfeiffer[becomerich.lab.u-ryukyu.ac.jp] […] cephalodactyly, included) 13 101400 Saethre-Chotzen syndrome (SCS) (Acrocephalosyndactyly, type III; ACS3) (ACS III) (Chotzen syndrome) (Acrocephaly, skull asymmetry and mild[becomerich.lab.u-ryukyu.ac.jp]

    Missing: Diffuse Osseous Demineralization
  • Arterial Tortuosity Syndrome

    […] subclavian arteries, ectasia of the innominate artery origin, and bilateral reduction of peripheral pulmonary branches. ii) Patient 1 showed elongated face, micrognathia, mild[ojrd.biomedcentral.com] A hyperextensible skin or mild cutis laxa can exist. Fingers are long and thin.[doi.org] blepharophimosis, downslanting palpebral fissures, beaked nose, high-arched palate. iii) Patient 2 showed elongated face, low-set and anteverted ears, down-slanting palpebral[ojrd.biomedcentral.com]

    Missing: Diffuse Osseous Demineralization
  • Kaufman Oculocerebrofacial Syndrome

    Definition A syndrome characterized by blepharophimosis, ptosis, mild upslanting of the palpebral fissures, epicanthus, ectodermal anomalies, developmental delay, and severe[uniprot.org] UniProtKB/Swiss-Prot : 76 Kaufman oculocerebrofacial syndrome: A syndrome characterized by blepharophimosis, ptosis, mild upslanting of the palpebral fissures, epicanthus,[malacards.org]

    Missing: Diffuse Osseous Demineralization
  • Hip Dysplasia Type Beukes

    […] syndactyly) (Saethre-Chotzen syndrome with eyelid anomalies, included) (Blepharophimosis, epicanthus inversus, and ptosis 3, formerly; BPES3, included) 14 101600 Pfeiffer[becomerich.lab.u-ryukyu.ac.jp] […] cephalodactyly, included) 13 101400 Saethre-Chotzen syndrome (SCS) (Acrocephalosyndactyly, type III; ACS3) (ACS III) (Chotzen syndrome) (Acrocephaly, skull asymmetry and mild[becomerich.lab.u-ryukyu.ac.jp]

    Missing: Diffuse Osseous Demineralization
  • Blepharoptosis

    Congenital Horner's syndrome which is characterized by mild ptosis, miosis, anhidrosis, and heterochromia.[eyewiki.aao.org] Blepharophimosis syndrome which is characterized by short palpebral fissures, congenital ptosis, epicanthus inversus, and telecanthus.[eyewiki.aao.org]

    Missing: Diffuse Osseous Demineralization
  • Blepharophimosis

    2 (a) Preoperative view of a 4-year-old girl (patient 8) with blepharophimosis syndrome; mild blepharophimosis (ratio 1.47).[nature.com] We report on a child and the mother who have blepharophimosis, ptosis, dental anomalies, mild hearing loss, and mental retardation.[ncbi.nlm.nih.gov] A 1-year-old boy, presenting with hypotonia, blepharophimosis, ptosis, a bulbous nose, mild psychomotor retardation, and epilepsy, was found to have mosaicism of chromosome[ncbi.nlm.nih.gov]

    Missing: Diffuse Osseous Demineralization

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