Literature DB >> 7815440

Mulvihill-Smith syndrome: case report and review.

O Bartsch1, K D Tympner, E Schwinger, R J Gorlin.   

Abstract

We report a 20 year old man with short stature, microcephaly, unusual facies, numerous pigmented naevi, hypodontia, immunodeficiency, and a high pitched voice. Tympner et al had assumed that the patient had a new syndrome of "progressive combined immunodeficiency and ectomesodermal dysplasia". We show here that the condition is identical to the Mulvihill-Smith syndrome (McKusick 176690), a progeroid disorder described in four or possibly five sporadic cases to date. We describe his clinical progress up to the age of 20 years. Our patient suffered from severe viral infections, allergic rhinitis and conjunctivitis, delayed puberty, visual loss, modest achievement in high school, and reactive depression. The immunological, facioskeletal, and dental abnormalities are presented in detail.

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Mesh:

Year:  1994        PMID: 7815440      PMCID: PMC1050081          DOI: 10.1136/jmg.31.9.707

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

1.  Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies.

Authors:  D E Elliott
Journal:  Birth Defects Orig Artic Ser       Date:  1975

2.  Another disorder with prenatal shortness of stature and premature aging.

Authors:  J J Mulvihill; D W Smith
Journal:  Birth Defects Orig Artic Ser       Date:  1975

3.  IBM-PC compatible software for establishing metacarpophalangeal pattern profiles.

Authors:  D Hosenfeld; F Hosenfeld; E Schaefer; W Grote
Journal:  Clin Genet       Date:  1991-05       Impact factor: 4.438

4.  A recognisable short stature syndrome with premature aging and pigmented naevi.

Authors:  M Baraitser; J Insley; R M Winter
Journal:  J Med Genet       Date:  1988-01       Impact factor: 6.318

5.  [Progressive combined immunity defect with ectomesodermal dysplasia (author's transl)].

Authors:  K D Tympner; B Belohradsky; R Eife; P K Klose
Journal:  Klin Padiatr       Date:  1978-11       Impact factor: 1.349

6.  Case report for syndrome identification.

Authors:  W Wong; M M Cohen; M Miller; S Pruzansky; I M Rosenthal; L M Solomon
Journal:  Cleft Palate J       Date:  1979-07

7.  An unidentified syndrome with abnormality of skin and hair.

Authors:  M K Shepard
Journal:  Birth Defects Orig Artic Ser       Date:  1971-06

Review 8.  Premature aging and immunodeficiency: Mulvihill-Smith syndrome?

Authors:  H Ohashi; M Tsukahara; I Murano; K Fujita; S Matsuura; Y Fukushima; T Kajii
Journal:  Am J Med Genet       Date:  1993-03-01
  8 in total
  2 in total

Review 1.  Immunodeficiencies Associated with Abnormal Newborn Screening for T Cell and B Cell Lymphopenia.

Authors:  Soma Jyonouchi; Artemio M Jongco; Jennifer Puck; Kathleen E Sullivan
Journal:  J Clin Immunol       Date:  2017-03-28       Impact factor: 8.317

Review 2.  The eleventh reported case of Mulvihill-Smith syndrome in the literature.

Authors:  Paulo Breinis; Flavio Geraldes Alves; Camila A E Alves; Rafael G Cintra; Débora Almeida; Priscila C Passarelli; Camila Domingues; Talita Gerbim; Régia Gasparetto; Luiz Carlos de Abreu; Vitor E Valenti; Adriana Gonçalves de Oliveira; Carlos Bandeira de Mello Monteiro; Rubens Wajnzstejn
Journal:  BMC Neurol       Date:  2014-01-07       Impact factor: 2.474

  2 in total

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