Literature DB >> 9800908

Microcephalic osteodysplastic primordial dwarfism type II: report of three cases and review.

F Majewski1, T O Goecke.   

Abstract

We report on three further patients with microcephalic osteodysplastic dwarfism type II. All children have marked intrauterine and postnatal growth failure, microcephaly, and mental and statomotor retardation. They are disproportionately short statured due to short limbs. Characteristic skeletal abnormalities are small iliac wings with flat acetabular angles, coxa vara, V-shaped distal femoral metaphyses, and triangular distal femoral epiphyses, as well as pseudoepiphyses of metacarpals, short first metacarpals, and brachymesophalangy V. At age 3 years, bilateral epiphyseolysis of the femoral heads occurred in case 1. Including our patients, 17 cases have been published so far. We review the clinical picture and the cause.

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Year:  1998        PMID: 9800908     DOI: 10.1002/(sici)1096-8628(19981102)80:1<25::aid-ajmg5>3.0.co;2-0

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Majewski dwarfism type II: an atypical neuroradiological presentation with a novel variant in the PCNT gene.

Authors:  Hamdan Alrajhi; Jubara Alallah; Aiman Shawli; Khalid Alghamdi; Fahad Hakami
Journal:  BMJ Case Rep       Date:  2019-05-30

2.  Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III.

Authors:  Gordana Juric-Sekhar; Raj P Kapur; Ian A Glass; Mitzi L Murray; Shawn E Parnell; Robert F Hevner
Journal:  Acta Neuropathol       Date:  2010-09-21       Impact factor: 17.088

Review 3.  Primordial dwarfism: overview of clinical and genetic aspects.

Authors:  Preeti Khetarpal; Satrupa Das; Inusha Panigrahi; Anjana Munshi
Journal:  Mol Genet Genomics       Date:  2015-09-01       Impact factor: 3.291

4.  Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms.

Authors:  Fei-Feng Li; Xu-Dong Wang; Min-Wei Zhu; Zhi-Hong Lou; Qiong Zhang; Chun-Yu Zhu; Hong-Lin Feng; Zhi-Guo Lin; Shu-Lin Liu
Journal:  Metab Brain Dis       Date:  2015-08-01       Impact factor: 3.584

5.  Clinical and functional characterization of a patient carrying a compound heterozygous pericentrin mutation and a heterozygous IGF1 receptor mutation.

Authors:  Eva Müller; Desiree Dunstheimer; Jürgen Klammt; Daniela Friebe; Wieland Kiess; Jürgen Kratzsch; Tassilo Kruis; Sandy Laue; Roland Pfäffle; Tillmann Wallborn; Peter H Heidemann
Journal:  PLoS One       Date:  2012-05-31       Impact factor: 3.240

6.  Majewski osteodysplastic primordial dwarfism type II: clinical findings and dental management of a child patient.

Authors:  Arslan Terlemez; Mustafa Altunsoy; Hakki Celebi
Journal:  J Istanb Univ Fac Dent       Date:  2015-01-31

7.  A 10-Year-Old Boy with Short Stature and Microcephaly, Diagnosed with Moyamoya Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II).

Authors:  Aurora Eslava; Montserrat Garcia-Puig; Raquel Corripio
Journal:  Am J Case Rep       Date:  2021-12-19

8.  A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II.

Authors:  Haifeng Liu; Na Tao; Yan Wang; Yang Yang; Xiaoli He; Yu Zhang; Yuantao Zhou; Xiaoning Liu; Xingxing Feng; Meiyuan Sun; Fang Xu; Yanfang Su; Li Li
Journal:  Mol Genet Genomic Med       Date:  2021-07-31       Impact factor: 2.183

  8 in total

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