Literature DB >> 8779319

New syndrome?: MCA/MR syndrome with multiple circumferential skin creases.

A M Elliott1, M Ludman, A S Teebi.   

Abstract

We describe a combination of multiple congenital anomalies, severe psychomotor retardation and symmetrical circumferential skin creases of arms and legs in a 4.5-year-old male. Craniofacial anomalies included: a high forehead, elongated face, bitemporal sparseness of hair, broad eyebrows, blepharophimosis, bilateral microphthalmia and microcornea, severe optic nerve hypoplasia, epicanthic folds, telecanthus, broad nasal bridge, puffy cheeks, microstomia, cleft palate, enamel hypoplasia, micrognathia, microtia with stenotic ear canals and posteriorly angulated ears. Head circumference was on the 10th centile and a CT scan showed dilated lateral ventricles. Intracranial pressure was not increased. Other abnormalities included: short stature, loose skin, hypotonia, pectus excavatum, inguinal and umbilical hernias, severe scoliosis, hypoplastic scrotum, long fingers and overlapping toes. Echocardiography showed tricuspid regurgitation. Chromosomes were apparently normal. Differentiation from "Michelin tire baby syndrome" and amniotic band sequence is discussed.

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Year:  1996        PMID: 8779319     DOI: 10.1002/(SICI)1096-8628(19960301)62:1<23::AID-AJMG5>3.0.CO;2-X

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


  6 in total

1.  New syndrome of congenital circumferential skin folds associated with multiple congenital anomalies.

Authors:  Lina Basel-Vanagaite; Eli Sprecher; Andrea Gat; Paul Merlob; Adi Albin-Kaplanski; Osnat Konen; Benjamin D Solomon; Maximilian Muenke; Karl-H Grzeschik; Lea Sirota
Journal:  Pediatr Dermatol       Date:  2011-10-13       Impact factor: 1.588

2.  Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

Authors:  Mala Isrie; Martin Breuss; Guoling Tian; Andi Harley Hansen; Francesca Cristofoli; Jasmin Morandell; Zachari A Kupchinsky; Alejandro Sifrim; Celia Maria Rodriguez-Rodriguez; Elena Porta Dapena; Kurston Doonanco; Norma Leonard; Faten Tinsa; Stéphanie Moortgat; Hakan Ulucan; Erkan Koparir; Ender Karaca; Nicholas Katsanis; Valeria Marton; Joris Robert Vermeesch; Erica E Davis; Nicholas J Cowan; David Anthony Keays; Hilde Van Esch
Journal:  Am J Hum Genet       Date:  2015-12-03       Impact factor: 11.025

Review 3.  A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

Authors:  T Cai; D A Tagle; X Xia; P Yu; X X He; L Y Li; J H Xia
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

4.  Familial Michelin tire baby syndrome.

Authors:  Arun Kumar Metta; S Ramachandra; Shilpa Manupati
Journal:  Indian J Dermatol       Date:  2012-01       Impact factor: 1.494

5.  Michelin Tire Baby Syndrome: A Rare Case with Review of Literature.

Authors:  Farheen Malik; Laraib Malik; Sina Aziz; Jawad Ahmed; Faryal Tahir
Journal:  Cureus       Date:  2019-09-10

6.  A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2.

Authors:  Jincai Feng; Xiaoping Lan; Jun Shen; Xiaozhen Song; Xiaojun Tang; Wuhen Xu; Xiang Ren; Hong Zhang; Guangjun Yu; Shengnan Wu
Journal:  Mol Genet Genomic Med       Date:  2020-01-05       Impact factor: 2.183

  6 in total

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