Neonatal diagnosis of circumferential skin creases

Author:

Cauzzo Chiara1ORCID,Chiavaroli Valentina23ORCID,Palka Bayard de Volo Chiara4ORCID,Petrucci Altea2,Topazio Teresa2,Di Donato Giulia1,Fiorentino Riccardo1ORCID,Chiarelli Francesco1,Di Valerio Susanna2

Affiliation:

1. Department of Pediatrics University of Chieti Chieti Italy

2. Neonatal Intensive Care Unit Pescara Public Hospital Pescara Italy

3. Liggins Institute, The University of Auckland Auckland New Zealand

4. Medical Genetics Unit SS Annunziata Hospital Chieti Italy

Abstract

AbstractBackgroundCircumferential skin creases is a rare and heterogeneous disorder characterized by multiple and redundant skin folds, which can present as an isolated feature or in association with other phenotypic anomalies. Here, we report the case of a newborn who immediately captured our attention because of his phenotype.CaseA male Caucasian infant was born at 39 weeks and 4 days of gestational age with an instrumental delivery, after a pregnancy characterized by threat of preterm birth at 32 weeks. Fetal ultrasounds were reported to be normal. The patient was the first child of non‐consanguineous parents. Anthropometry at birth: weight 3.590 kg (0.57 SDS); length 53 cm (1.73 SDS); cranial circumference 35.5 cm (0.83 SDS). Clinical examination soon after birth revealed multiple, asymmetric and deep skin folds involving forearms, legs and lower eyelids (right > left). These folds seemed not to cause any physical discomfort. In addition, hypertrichosis, micrognathia, low‐set ears and a thin, down‐turned border of upper lip were observed. Cardio‐respiratory, abdominal and neurological examination was unremarkable. There was no family history of similar appearance or other physical abnormalities. Given the clinical picture, an array‐CGH was performed, which was normal. A genetic counseling was requested and Circumferential Skin Creases disorder was diagnosed based on the typical cutaneous involvement and, given the absence of other clinical signs, it was supposed a benign evolution, with skin folds tending to disappear over time. In addition, the baby's DNA was requested for a targeted genetic analysis, which resulted negative.ConclusionsThis clinical case underlines the need of performing a detailed neonatal physical examination in order to realize a timely diagnostic approach. Our patient presented with multiple skin folds, facial dysmorphism but normal systemic and neurological examination. Anyways, since Circumferential Skin Creases may be associated with later neurological symptoms, a regular reevaluation is recommended.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

Reference15 articles.

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2. Michelin tire baby syndrome: Familial constriction bands during infancy and early childhood in four generations

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5. Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type

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