Literature DB >> 2703235

A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.

L O Langer1, J Cervenka, M Camargo.   

Abstract

Two siblings with a short-limb dwarfing condition which we call acromesomelic dysplasia, Hunter-Thompson type are reported. Abnormalities are limited to the limbs and limb joints in this severe form of dwarfism. The middle and distal segments of the limbs are most affected. The lower limbs are more affected than the upper. We are aware of one previously published case of this entity reported by A. G. W. Hunter and M. W. Thompson in 1976. Dislocations of the elbows and ankles were present in all three patients and dislocations of the hips and knees in two. One of the siblings who did not have hip and knee dislocations clinically resembled Grebe chondrodysplasia, another severe acromesomelic dwarfing condition. However, radiological analysis suggests that while acromesomelic dysplasia, Hunter-Thompson type and Grebe chondrodysplasia are related, they are not identical. Grebe chondrodysplasia has been established as an autosomal recessive trait. It appears probable that the entity we describe has the same mode of genetic transmission.

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Year:  1989        PMID: 2703235     DOI: 10.1007/BF00283684

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  Nonlethal achondrogenesis (Grebe-Quelce-Salgado type) in two Puerto Rican sibships.

Authors:  J M García-tcastro; A Pérez-Comas
Journal:  J Pediatr       Date:  1975-12       Impact factor: 4.406

2.  A NEW TYPE OF DWARFISM WITH VARIOUS BONE APLASIAS AND HYPOPLASIAS OF THE EXTREMITIES.

Authors:  A QUELCE-SALGADO
Journal:  Acta Genet Stat Med       Date:  1964

3.  CONGENITAL DEFORMITIES OF LIMBS IN DIFFERENT MEMBERS OF A FAMILY.

Authors:  K JOHN; M P GUNDAPPA
Journal:  J Indian Med Assoc       Date:  1963-12-01

4.  Grebe chondrodysplasia and similar forms of severe short-limbed dwarfism.

Authors:  G Romeo; J Zonana; R S Lachman; J M Opitz; C I Scott; J W Spranger; D L Rimoin
Journal:  Birth Defects Orig Artic Ser       Date:  1977

5.  Heterogeneity of nonlethal severe short-limbed dwarfism.

Authors:  G Romeo; J Zonana; D L Rimoin; R S Lachman; C I Scott; E G Kaveggia; J W Spranger; J M Opitz
Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

6.  A rare genetic syndrome.

Authors:  A Quelce-Salgado
Journal:  Lancet       Date:  1968-06-29       Impact factor: 79.321

7.  Grebe chondrodysplasia in three generations of an Andhra family in India.

Authors:  P Meera Khan; A Khan
Journal:  Prog Clin Biol Res       Date:  1982

8.  Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.

Authors:  A G Hunter; M W Thompson
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

9.  Grebe chondrodysplasia and brachydactyly in a family.

Authors:  D Kumar; D Curtis; C E Blank
Journal:  Clin Genet       Date:  1984-01       Impact factor: 4.438

  9 in total
  8 in total

Review 1.  Changes in clinical practice with the unravelling of diseases: connective-tissue disorders.

Authors:  J Spranger
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

Review 2.  TGF-β Family Signaling in Connective Tissue and Skeletal Diseases.

Authors:  Elena Gallo MacFarlane; Julia Haupt; Harry C Dietz; Eileen M Shore
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-11-01       Impact factor: 10.005

3.  Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.

Authors:  S G Kant; A Polinkovsky; S Mundlos; B Zabel; R T Thomeer; H M Zonderland; L Shih; A van Haeringen; M L Warman
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

4.  Neonatal Death Dwarfism in a Girl with Distinctive Bone Dysplasia Compatible with Grebe Chondrodysplasia: Analysis by CT Scan-based Phenotype.

Authors:  Ali Al Kaissi; Farid Ben Chehida; Rudolf Ganger; Franz Grill
Journal:  J Clin Imaging Sci       Date:  2014-09-29

5.  Heads, Shoulders, Elbows, Knees, and Toes: Modular Gdf5 Enhancers Control Different Joints in the Vertebrate Skeleton.

Authors:  Hao Chen; Terence D Capellini; Michael Schoor; Doug P Mortlock; A Hari Reddi; David M Kingsley
Journal:  PLoS Genet       Date:  2016-11-30       Impact factor: 5.917

Review 6.  "Lessons from Rare Forms of Osteoarthritis".

Authors:  Rebecca F Shepherd; Jemma G Kerns; Lakshminarayan R Ranganath; James A Gallagher; Adam M Taylor
Journal:  Calcif Tissue Int       Date:  2021-08-21       Impact factor: 4.333

7.  The role of Gdf5 regulatory regions in development of hip morphology.

Authors:  Ata M Kiapour; Jiaxue Cao; Mariel Young; Terence D Capellini
Journal:  PLoS One       Date:  2018-11-02       Impact factor: 3.240

8.  Joint disease-specificity at the regulatory base-pair level.

Authors:  Pushpanathan Muthuirulan; Dewei Zhao; Mariel Young; Daniel Richard; Zun Liu; Alireza Emami; Gabriela Portilla; Shayan Hosseinzadeh; Jiaxue Cao; David Maridas; Mary Sedlak; Danilo Menghini; Liangliang Cheng; Lu Li; Xinjia Ding; Yan Ding; Vicki Rosen; Ata M Kiapour; Terence D Capellini
Journal:  Nat Commun       Date:  2021-07-06       Impact factor: 14.919

  8 in total

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