Smith's Recognizable Patterns of Human Malformation
This user-friendly 5th Edition provides concise but complete information on numerous common and rare disorders that cause human malformation. Includes an outline of the salient features of each condition, as well as material on natural history, etiology, and pathogenesis. The text is accompanied by helpful illustrations and reference lists. Organized to allow for easy access to essential information.
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Recognizable Patterns of Malformation
B VERY SMALL STATURE NOT SKELETAL DYSPLASIA
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50 per cent ABNORMALITIES Growth achondroplasia agenesis and/or anomalies Arch associated atresia Autosomal dominant Autosomal recessive birth bones cardiac defects cells Child Chondrodysplasia Punctata chromosome cleft lip cleft palate Clin clinical congenital Courtesy of Dr Craniofacial crease cryptorchidism Deletion diagnosis disorder distal drome Duplication Dysostosis early ears Ectodermal Dysplasia epiphyses ETIOLOGY facial facies Fanconi Pancytopenia fected females fifth finger FIGURE Frequent gene Genet Gorlin growth deficiency hair height age hernia hypertelorism hypoplasia hypoplastic hypotonia infant joint Limbs males malformation mental deficiency mental retardation Metaphyseal Microcephaly micrognathia mild morphogenesis multiple mutations nasal bridge NATURAL HISTORY neonatal normal OCCASIONAL ABNORMALITIES occur ocular Opitz Osteogenesis Imperfecta palpebral fissures patients pattern Pediatr permission phalanges phenotype polydactyly posterior postnatal prominent Pterygium References renal reported ribs risk scoliosis septal defect Sequence severe short Skeletal skin Spectrum stature stenosis syndactyly syndrome synostosis tion tissue toes Trisomy 18 twins Type usually variable vertebral X-linked
Disorders of Development and Learning, Volume 1
No preview available - 2003
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