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Decoding Human Personality Through Dermatoglyphics.
Cureus
October 2022
Department of General Surgery, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences (Deemed to be University), Wardha, IND.
Background Dermatoglyphics refers to the study of epidermal ridges or patterns on fingers (fingerprints) and palms (palmprints). These epidermal ridges grow concurrently with a fetus's neural development during the intrauterine stage of life. Determining genetic anomalies using dermatoglyphics can help identify congenital deformities, various other medical conditions, and how the brain functions well ahead of time.
View Article and Find Full Text PDFPrevalence of palmar crease patterns and associated factors among students at University of Gondar, Northwest Ethiopia.
Anat Cell Biol
June 2022
Department of Human Anatomy, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Palmar creases are unique, permanent, and genetically controlled morphological variables. Recognizing palmar crease types are important for personal identification, criminal investigations, and diagnosis of congenital diseases. This study aimed to reveal the anthropological characteristics as well as contribute to the diagnosing of congenital disease of Ethiopian people.
View Article and Find Full Text PDFA Novel Intronic Variant as a Cause of Kabuki Syndrome: A Case Report.
Appl Clin Genet
October 2021
Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Valle del Cauca, Colombia.
Kabuki syndrome (KS) is an autosomal dominant genetic disorder in which most cases are caused by de novo mutations. KS type 1 is caused by mutations in (OMIM: #147920) and is more common. KS type 2 is caused by mutations in (OMIM: #300867).
View Article and Find Full Text PDFAssociation between ABO, Rh blood groups, lip and dermatoglyphic patterns, and nonsyndromic oral clefts: A case-control study.
J Indian Soc Pedod Prev Dent
April 2021
Department of Public Health Dentistry, Meenakshi Ammal Dental College, Chennai, Tamil Nadu, India.
Objective: The objective of the study is to determine the association between nonsyndromic oral clefts (OC) in children and ABO, Rh blood groups, lip, and dermatoglyphic patterns of their unaffected parents.
Methods: This case-control study was conducted at a tertiary cleft center in Chennai, India, among 240 individuals comprising 80 units (40 cases and controls, respectively). Each unit (triad) was constituted by a child (0-12 years of age) either born with nonsyndromic OC (cases) or with no diagnosed congenital anomaly (control) and their unaffected parents (mother and father).
Facial Dysmorphisms, Macrodontia, Focal Epilepsy, and Thinning of the Corpus Callosum: A Rare Mild Form of Kabuki Syndrome.
J Pediatr Genet
March 2021
Pediatric Unit, Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy.
Kabuki syndrome (KS) is a rare genetic condition with multiple congenital abnormalities and developmental delay. The cardinal manifestations of KS include characteristic facial features, intellectual disability, skeletal defects, dermatoglyphic abnormalities, and postnatal growth deficiencies. Cardiac and urological malformations are commonly present in patient with KS, as well as language deficits and immunological abnormalities.
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