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Differential Diagnosis For Particular physiognomy/Odd looking kids: Hereditary, Familial, Genetic Disorders

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Particular physiognomy/Odd looking kids
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Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes: Ataxia-telangiectasia; Basal cell nevus syndrome (Gorlin); Cleidocranial digital dysostosis; Fragile X syndrome/X-linked retardation; Nephritis, hereditary (Alports); Neurofibromatosis; Osteogenesis imperfecta; Pseudo-pseudohypoparathyroidism; Chromosome 22q13.3 deletion syndrome (22q13.3); Jackson-Weiss Craniosynostosis syndrome; Jarcho-Levin Spondylocostal dysplasia Syndrome; Johanson Blizzard genetic syndrome (unco); Juberg Marsidi Genetic syndrome (unco); Myhre Syndrome; Neonatal Progeria Familial (Wiedemann); Pitt syndrome (4p16.3); Pallister Hall Syndrome; Pallister W Syndrome; Pseudohypoparathyroidism; Acrocephalosyndactyly type III syndrome; Apert syndrome; Bird-headed dwarf of Seckel; Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3); Cockayne syndrome; Cryptophthalmos (Fraser) syndrome; Dolichospondylic dysplasia; Facial ectodermal dysplasia (Setleis); Facioscapulohumeral muscular dystrophy; Hypothalamic hypogonadism, Kallman's; Leprechaunism; Lipodystrophy, generalized; Myotonia atrophica (Steinert's disease); Oculocerebrorenal dystrophy/Lowe syndrome; Osteodysplasia, familial (Melnick Needles); Schwartz-Jampel syndrome; Scott's Craniodigital syndrome; SHORT syndrome (Rieger anomaly plus); Simpson dysmorphia syndrome; Smith-Lemli-Opitz syndrome; Stickler syndrome; Treacher Collins syndrome; Waardenburg-Klein syndrome; Williams syndrome/Elfin facies; Winchester syndrome; 18p chromosome deletion complex; Abducted thumbs syndrome; Acrocallosal syndrome (ACS); Adducted thumbs-Mental retardation syndrome; Andermann Syndrome; Brooks syndrome; Chudley Syndrome 1; Conradi-Hunermann Syndrome; Craniofrontonasal Syndrome (CFNS); Curran acrorenal syndrome; Faciocardiorenal Syndrome (Eastman-Bixler); Kabuki make-up syndrome; Michelin tire baby syndrome; Neu Laxova Syndrome; Neuhauser Syndrome; Reiger Syndrome; Say Syndrome 1

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