failure of development of the primitive lung bud leads to an extremely rare congenital anomaly with a prevalence of 34 per 10 lac live births termed pulmonary aplasia. in half of such cases, associated congenital malformations of the cardiovascular, skeletal, gastrointestinal, or genitourinary systems are present. the mayer-rokitansky-küster-hauser (mrkh) syndrome is defined as the congenital a...

Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome: aplasia cutis congenita and epibulbar dermoids. Our case expands the clinical spectrum of the di...

Hyperthyroidism is more common in women and the sensitivity of thyroid function changes during pregnancy. Excess levels hormones thioamides have a major impact on maternal fetal outcomes. Our aim was to perform an extensive literature review provide relevant details concerning analytical clinical aspects potential effects two main drugs used (methimazole propylthiouracil) newborns. A thorough c...

Abstract Background Extracranial congenital skin defects, defined as aplasia cutis congenita (ACC), are a rare clinical entity. The form of presentation varies among patients according to the causal agent and point during pregnancy at which defect occurs. We present series cases noncranial ACC, analysing its possible etiopathogenesis evolution lesions. Materials methods This is retrospective re...

background cutis marmorata telangiectatica congenita (cmtc) is a sporadic congenital skin vascular abnormality. significant number of patients has other congenital anomalies. case report we report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. besides, microretrognatia and asymm...