Sentence examples for congenital features from inspiring English sources

Histological examination of the nevi at autopsy and revision of previously removed CMN, demonstrated compound melanocytic nevi with congenital features, without signs of malignancy.

Skin lesions from the neck, scalp, and arm were previously excised and diagnosed as intradermal and compound nevi with congenital features.

The latter is a congenital feature that has been linked with instability of the skeleton and with scoliosis [ 5].

It is of interest to understand the onset of the expression of such proteins related to the congenital feature of the disease.

In addition, these data show that multidrug resistance is not a congenital feature of E. coli, and that drug use and resistance are closely related temporally.

The newborns with congenital anomalies/dysmorphic features, multiple births and gestational age of less than 37 completed weeks (pre term babies) were excluded.

It is characterized by a variety of dysmorphic features, congenital malformations, and other health problems.

The selection criteria of the patients, in addition to the intellectual disability or autism spectrum disorders (ASD), were the presence of congenital abnormalities, dysmorphic features, and/or a positive family history for neurodevelopmental disorders or congenital abnormalities.

In the absence of any specific structural changes (including significant increase of central nuclei, rods, cores, multi/mini-cores or obvious dystrophic type changes) the main differential diagnosis of the findings includes congenital myopathy with features of CFTD and the possibility of biopsy at too young of an age to visualize other specific pathology such as CNM.

DSCAM has been proposed to contribute to the congenital heart disease feature of DS, and it is possible that mis-regulation of a large number of adhesion-related genes through epigenetic modification may explain the increased risk in the DS population [ 45].

With the publication of additional case reports, and the clinical descriptions of large cohorts of individuals with 1p36 deletions, a pattern of characteristic functional deficits, congenital anomalies, and physical features associated with 1p36 deletions emerged.