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Acro-callous syndrome: A case report.

A Lamrissi¹, F E Madri², M Charkaoui²

¹Maternity Service, Mother and Child Hospital Abderrahim Harouchi, University Hospital IBN ROCHD of Casablanca, Morocco; Gynecology Obstetric Department, Faculty of Medicine and Pharmacy of Casablanca, Hassan 2 University of Casablanca, Morocco; Biology and Health Laboratory (LBS), Hassan 2 University of Casablanca, Morocco.

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Summary

This summary is machine-generated.

Acrocal syndrome is a rare genetic disorder diagnosed via fetal imaging. Four diagnostic criteria help confirm acrocal syndrome and distinguish it from other malformation syndromes.

Keywords:

Acrocallous syndrome Antenatal diagnosis Embryo-fetopathy Polymalformative syndrome

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Area of Science:

Medical Genetics
Prenatal Diagnosis
Fetal Imaging

Background:

Acrocal syndrome is a malformative syndrome with unknown prevalence.
Diagnosis relies on fetal morphological ultrasound and magnetic resonance imaging.
The condition exhibits autosomal recessive genetic transmission.

Purpose of the Study:

To establish diagnostic criteria for acrocal syndrome.
To differentiate acrocal syndrome from other polymalformative syndromes.

Main Methods:

Utilizing morphological ultrasound and magnetic resonance imaging for diagnosis.
Establishing four key diagnostic criteria.

Main Results:

Defined criteria for affirming acrocal syndrome.
Provided a method to exclude similar polymalformative syndromes.

Conclusions:

The established criteria aid in the accurate diagnosis of acrocal syndrome.
Distinguishing acrocal syndrome from other conditions is crucial for appropriate management.