Introduction Congenital contractures in the newborn are actually common, ranging from 1 : 100 to 1 : 200 for some types of contractures that include clubfeet, hip dislocations, and multiple congenital contractures (MCCs). Talipes equinovarus or clubfoot is an abnormality of the foot position. It may be positional, an isolated abnormality, or part of a larger constellation of abnormalities as seen in many genetic syndromes. Clubfoot resulting from in utero…

Introduction The development of the fetal skull is a complex process involving intramembranous and endochondral ossification. The fetal cranium comprises bony plates that are joined together by areas of dense fibrous tissue termed cranial sutures, comprised of the sagittal, coronal, lambdoid, and metopic sutures ( Fig. 62.1 ). The membranous sutures allow for expansion of the calvaria to accommodate rapid human brain growth prenatally and postnatally.…

Introduction Routine second-trimester ultrasound (US) examination typically involves only a cursory evaluation of the extremities, documenting the presence or absence of the arms and legs; however, comprehensive evaluation of the fetal extremities often yields critical information. Anomalies of the hands are difficult to diagnose, and malformations range from subtle deformities, such as isolated fifth-finger clinodactyly, to complete absence of extremities, as seen in phocomelia syndromes such…

Introduction Spinal malformations associated with vertebral segmentation defects and progressive fusions are seen in numerous syndromes, particularly those associated with skeletal dysplasias. Among spinal malformations, one of the best-described constellation of findings is Klippel-Feil syndrome (KFS), a triad of short neck, low posterior hairline, and limitation of head and neck movements. The original case report described a patient with significant kyphosis secondary to congenital fusions of…

Introduction Among newborns with birth defects, approximately one-third show craniofacial abnormalities, which cause significant morbidity and mortality. More than 700 distinct craniofacial syndromes have been described to date. Facial dysostoses can be divided into two types: mandibulofacial dysostoses (MFDs) and acrofacial dysostoses (AFDs). MFDs have typically no limb defects, while AFDs are associated with limb abnormalities. At least eight MFDs have been described, with the most…

Introduction Achondrogenesis II, hypochondrogenesis, platyspondylic Torrance type, spondyloepiphyseal dysplasia congenita (SEDC) ( Chapter 56 ), Kniest dysplasia, spondyloepimetaphyseal dysplasia, Strudwick type, Legg-Calve-Perthes disease, spondyloperipheral dysplasia, spondyloepiphyseal dysplasia with metatarsal shortening (Czech type), autosomal dominant spondyloarthropathy, and Stickler syndrome form the type II collagen disorder group. This group is a continuous spectrum of disorders, some of which manifest in the prenatal period, some much later in life.…

Introduction Spondyloepiphyseal dysplasias are rare, nonlethal disorders of bone growth. These disorders primarily affect the spine (spondylo-) and the ends of the long bones (epiphyseal), resulting in a short-trunk dwarfism. These disorders are clinically and genetically heterogeneous. Some spondyloepiphyseal dysplasias manifest in the prenatal period, including spondyloepiphyseal dysplasia congenita (SEDC), whereas others manifest in childhood. Other spondyloepiphyseal dysplasias are diagnosed in later life as early-onset arthropathy.…

Introduction The short-rib polydactyly syndromes (SRPSs) are a genetically heterogeneous group of autosomal recessive skeletal disorders. Characteristic findings in SRPS include short horizontal ribs, shortened appendicular long bones limbs, and polydactyly. Historically, four distinct SRPS types have been recognized : SRPS I (Saldino-Noonan syndrome) SRPS II (Majweski syndrome) SRPS III (Verma-Naumoff syndrome) SRPS IV (Beemer-Langer syndrome) Currently the SRPSs are classified as “ Ciliopathies with major…

Introduction Russell-Silver syndrome (RSS) or Silver-Russell syndrome is one of the growth deficiency disorders that form part of the increasing group of congenital imprinting disorders. RSS is characterized by severe intrauterine and postnatal growth restriction. Other abnormalities include relative macrocephaly, hemihypertrophy (one side of the body is larger than the other), fifth finger clinodactyly, and triangular-shaped facies. RSS is genetically heterogeneous and the phenotype can vary.…

Introduction Ultrasound (US) evaluation of a fetus with a radial ray defect is a difficult diagnostic dilemma because the defect may be isolated, but can also result from chromosomal aneuploidy, teratogenic exposure, and more than 200 distinct genetic syndromes, including skeletal dysplasias, particularly those associated with mesomelia. Radial aplasia or hypoplasia is a rare abnormality occurring in 2 : 10,000 liveborns, but more common than isolated ulnar abnormalities.…

Introduction Osteogenesis imperfecta (OI), a disorder of bone characterized by hypomineralization of the skeleton, was the first disorder proposed to be due to a defect in collagen. It is characterized by life-long bone fragility and fracture predisposition. Other features, depending on the type of OI, may include blue sclerae, hearing loss, hypermobility of joints, and abnormal dentition. OI is marked by considerable clinical and genetic heterogeneity.…

Introduction Hypophosphatasia (HPP) is an autosomal recessive disorder that is characterized by poor mineralization of bones and teeth. There are at least six phenotypes, which are distinguished from each other by age at diagnosis, inheritance pattern, and prognosis. The primary forms are named for age at diagnosis and include perinatal (lethal), infantile, childhood, and adult HPP. In most cases that are diagnosed perinatally, infants are either…

Introduction Fibroblast growth factor receptor 3 (FGFR3) disorders compromise of a spectrum of disorders that include thanatophoric dysplasia, achondroplasia, and hypochondroplasia, among other rare disorders such as severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), and craniosyntoses syndromes. They are all inherited as autosomal dominant disorders due to heterozygosity for mutations in FGFR3 . Achondroplasia is the most frequent cause of nonlethal dwarfism and is…

Introduction Diastrophic dysplasia (DTD) is an autosomal, recessively inherited skeletal dysplasia characterized by short limbs, normal-sized skull, cleft palate in one-third of patients, characteristic swelling of the pinnae cartilage, contractures of the large joints with deformities, spinal abnormalities (scoliosis, exaggerated lumbar lordosis, cervical kyphosis), and a distinct brachydactyly associated with the characteristic “hitchhiker” thumbs. Newborns with DTD have an increased risk of mortality in the neonatal…

Introduction Chondrodysplasia punctata refers to a group of skeletal dysplasias that are characterized primarily by punctate calcifications in cartilage (calcific stippling). These disorders are characterized by short-limb dwarfism, spinal abnormalities, facial dysmorphisms, joint contractures, skin lesions, and occasionally cardiac malformations. There are multiple types of chondrodysplasia punctata, and there is extensive locus and allelic heterogeneity. Disorder Definition The term chondrodysplasia punctata describes a group of osteochondrodysplasias…

Introduction Campomelic dysplasia (CD) is a skeletal dysplasia characterized by abnormal facies, multiple congenital anomalies, a typical pattern of skeletal abnormalities, and frequent male-to-female sex reversal. Newborns with CD often die as a result of respiratory insufficiency and congenital anomalies. A small subset of individuals with clinical features of CD lack characteristic long bone bowing and are classified as having acampomelic campomelic dysplasia. CD results from…