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all cases are of the equinovarus clubfoot variety (ie, the foot turns downward and inward) Usually both feet are affected Multiple incidence in one family may occur Several explanations of cause and pathogenesis have been offered: fetal malposition, an embryonic abnormality of tarsal and metatarsal bones, a primary defect in nerves or anterior horn cells of the spinal cord, or a congenital dystrophy of muscle No one theory explains all cases and available pathologic data exclude a single cause and pathogenesis In some instances clubfoot is the only recognizable congenital abnormality, but more often it occurs as a manifestation of generalized arthrogryposis (see later) and is an indicator of a more widespread involvement of the central nervous system (See Kakulas and Adams and also Banker for pertinent literature on the subject) Congenital Torticollis (Wryneck) This disorder begins during the rst months of life and, unlike the torticollis of adults discussed in Chap 6, it is not the result of a dystonia but instead is due to congenital shortening of the sternocleidomastoid muscle, which is rm and taut The head is inclined to one side and the occiput slightly rotated to the side of the affected muscle This disorder is nonfamilial and is usually ascribed to injury of the sternocleidomastoid at birth Whether the injury is a purely mechanical one to the muscle itself or is due to ischemia stemming from arterial or venous occlusion (or an entirely different cause) is not totally clear It often gives rise to a sternocleidomastoid tumor (actually a pseudotumor) that appears, on exploration, as a pale, spindle-shaped swelling of the muscle belly The histologic ndings are similar to those of Volkmann contracture, ie, replacement of the muscle bers by relatively acellular connective tissue, suggesting that an ischemic mechanism underlies the defect in some cases barcode software for excel free download Get Barcode Software - Microsoft Store
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Use mature Excel 2D Barcode Add- In to generate and insert QR Code, Data Matrix, PDF417, etc, on Excel spreadsheet. Download Free Trial Package | User ... It is well known that some individuals are born without certain muscles This pertains not only to certain inconstant and functionally unimportant muscles, such as the palmaris longus, but also to more constant and substantial ones as well The muscles found to be absent most frequently are the pectoralis, trapezius, serratus anterior, and quadriceps femoris, but many others are missing in isolated cases Congenital absence of muscle is usually associated with congenital anomalies of neighboring nonmuscular tissues For example, congenital absence of the pectoral muscle is often accompanied by aplasia or hypoplasia of the mammary or of syndactyly and microdactyly Agenesis of the pectoral muscle may also be associated with scoliosis, webbed ngers, and underdevelopment of the ipsilateral arm and hand (Poland syndrome) Another unusual syndrome consists of congenital absence of portions of the abdominal muscles ( prune belly ), often in association with arthrogryposis and a defect of ureters, bladder, and genital organs There is also an association in a few cases between a congenital amyoplasia and facioscapulohumeral muscular dystrophy In another group of restricted palsies, the essential abnormality appears to lie in the central nervous system (nuclear amyotrophies) One of the most frequent is congenital ptosis due to an inborn defect of the innervation of the levator palpebrae muscles Complete paralysis of all muscles supplied by the oculomotor nerve, due apparently to hypoplasia of the third nerve nuclei, may be observed in several members of a family and occasionally in only one member As discussed in Chap 14, congenital Horner syndrome may be familial; it is associated with depigmentation of the iris (heterochromia iridis) Bilateral abducens palsy is often associated with bifacial palsy in the newborn and is known as the Mob ius syndrome; this usually nonfamilial anomaly, the cause of which is thought to be a nuclear hypoplasia or aplasia, is discussed with the developmental disorders (page 873) In these familial nuclear amyotrophies the muscles develop independently of the nervous system but have no prospect of attaining their natural growth and function and indeed of surviving because of failure of innervation It is a kind of congenital denervation hypotrophy Of course, a primary muscle defect may also give rise to bifacial weakness, as in facioscapulohumeral muscular dystrophy Beta-Hydroxy Acid (Salicylic Acid) barcode in excel 2003 free Microsoft Excel Barcode Add-in Tutorial for 2003, 2007, and 2010 ...
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