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Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features of the...
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Cushing syndrome refers to the collection of clinical manifestations that arise when tissues are exposed to excessive amounts of cortisol or cortisol-like medications over an extended period. Cortisol, a glucocorticoid produced by the adrenal cortex, regulates metabolism, immune responses, and the body’s adaptation to stress. When its concentration remains chronically elevated, these physiological pathways become dysregulated, resulting in the characteristic features of the syndrome.Exogenous...
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Related Experiment Video

Updated: Jul 10, 2026

Modification of the Treatment Methods for Wasting Marmoset Syndrome with Tranexamic Acid and Supportive Measures
03:07

Modification of the Treatment Methods for Wasting Marmoset Syndrome with Tranexamic Acid and Supportive Measures

Published on: July 12, 2024

Mowat-Wilson syndrome.

Livia Garavelli1, Paola Cerruti Mainardi

  • 1Clinical Genetics Unit, Obstetric and Pediatric Department, S, Maria Nuova Hospital, Reggio Emilia, Italy. garavelli.livia@asmn.re.it

Orphanet Journal of Rare Diseases
|October 26, 2007
PubMed
Summary

Mowat-Wilson syndrome (MWS) is a genetic disorder caused by ZEB2 gene mutations, characterized by distinct facial features, intellectual disability, and congenital anomalies. Early diagnosis and multidisciplinary intervention are crucial for managing MWS patients.

Area of Science:

  • Genetics
  • Pediatrics
  • Medical Genetics

Background:

  • Mowat-Wilson syndrome (MWS) is a rare multiple congenital anomaly syndrome.
  • It presents with a characteristic facial phenotype, intellectual deficiency, epilepsy, and variable congenital malformations.
  • MWS is caused by heterozygous mutations or deletions in the ZEB2 gene.

Purpose of the Study:

  • To describe the clinical features and genetic basis of Mowat-Wilson syndrome.
  • To highlight the importance of facial phenotype in diagnosis.
  • To emphasize the need for early intervention and multidisciplinary care.

Main Methods:

  • Review of reported MWS cases and genotype-phenotype analysis.
  • Genetic analysis of ZEB2 gene mutations and deletions.

Related Experiment Videos

Last Updated: Jul 10, 2026

Modification of the Treatment Methods for Wasting Marmoset Syndrome with Tranexamic Acid and Supportive Measures
03:07

Modification of the Treatment Methods for Wasting Marmoset Syndrome with Tranexamic Acid and Supportive Measures

Published on: July 12, 2024

  • Clinical assessment of patient phenotypes, including facial features and congenital anomalies.
  • Main Results:

    • Facial gestalt and delayed psychomotor development are constant features of MWS.
    • Congenital malformations such as Hirschsprung disease, genitourinary anomalies, and heart defects are variable.
    • ZEB2 haploinsufficiency is the primary pathological mechanism, with truncating mutations and whole gene deletions being common.

    Conclusions:

    • The distinct facial phenotype is a key diagnostic hallmark for MWS, guiding ZEB2 mutational analysis.
    • MWS is likely under-diagnosed, especially in patients without Hirschsprung disease.
    • Early and comprehensive multidisciplinary management, including rehabilitation, is essential for improving outcomes in MWS patients.