What does this research mean for the field?

EEC syndrome manifests as a triad of ectrodactyly, ectodermal dysplasia, and cleft lip/palate across sexes and racial backgrounds, including familial occurrence among siblings. Novelty: ClaimNovelty.INCREMENTAL. Consensus alignment: ConsensusAlignment.NEUTRAL.

June 1, 1974Archives of Pediatrics and Adolescent Medicine

The EEC Syndrome

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Key result

New case series characterizes EEC syndrome across six patients, including familial presentation in two sisters.

Design

Case series

Authors

CPConstance Pries

Discussion

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Implication

Broadens EEC syndrome phenotypic data with six cases; leaves open questions on genetics and management pending larger studies.

Structured PICO

Population

6 patients with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft of the lip and palate), including 5 white and 1 black patient, 4 females and 2 males (including 2 sisters).

This report expands the clinical literature on EEC syndrome by describing six new cases.

Cite This Study

Constance Pries (1974) studied this question. Six new cases of EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft lip/palate) were described in four females, including two sisters, and two males.

synapsesocial.com/papers/6ab46df6ba2a4ba258208954 https://doi.org/10.1001/archpedi.1974.02110250066009

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The EEC Syndrome

Discussion

Member takes

Implication

Structured PICO

Cite This Study

The EEC Syndrome

Discussion

Member takes

Implication

Structured PICO

Cite This Study

Also Consider

Also Consider