Literature DB >> 4950920

Multiple mucosal neuromas, pheochromocytoma, medullary carcinoma of the thyroid and marfanoid body build with muscle wasting: reexamination of a syndrome of neural crest malmigration.

R J Gorlin, R A Vickers.   

Abstract

Initially described in part by Wagenmann and by Froboese almost 50 years age, the syndrome of a) multiple mucosal neuromas, b) pheochromocytoma, c) medullary carcinoma of the thyroid and d) marafanoid build with muscle wasting of the limbs, was enlarged by Williams and Pollock, Gorlin et al, Schimke et al and Levy et al.

Entities:  

Mesh:

Year:  1971        PMID: 4950920

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  6 in total

1.  Pituitary adenoma, primary parathyroid hyperplasia and papillary (non-medullary) thyroid carcinoma. A case of multiple endocrine neoplasia (MEN).

Authors:  H Dralle; E Altenähr
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1979-02-09

2.  Hypertrophy of peripheral nerves in the syndrome of multiple mucosal neuromas, endocrine tumours and Marfanoid habitus. Autonomic disturbances and sural nerve findings.

Authors:  E Joosten; A Gabreëls-Festen; M Horstink; F Gabreëls; H Jaspar; J Korten; H Vingerhoets
Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

3.  Multiple mucosal neuromas, pheochromocytoma, medullary carcinoma of the thyroid and marfanoid body build with muscle wasting. Syndrome of hyperplasia and neoplasia of neural crest derivatives--an unitarian concept.

Authors:  R J Gorlin; B L Mirkin
Journal:  Z Kinderheilkd       Date:  1972

Review 4.  Mucosal neuromata syndrome (MEN type IIb (III)).

Authors:  J P Fryns; K Chrzanowska
Journal:  J Med Genet       Date:  1988-10       Impact factor: 6.318

Review 5.  Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).

Authors:  P J Morrison; N C Nevin
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

6.  A unique association of Marfan syndrome with craniofacial hypoplasia, oligophrenia and severe microphthalmia.

Authors:  G Capocchi; R Fausti; M Zamponini; N Caputo; A Rossi
Journal:  Ital J Neurol Sci       Date:  1988-08
  6 in total

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