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161 Possible Causes for Juvenile Familial Leg Ulcers, Mild Midface Hypoplasia

  • Leukoencephalopathy - Metaphyseal Chondrodysplasia Syndrome

    Ulcers, Familial, of Juvenile Onset OMIM:220111 Leigh Syndrome, French Canadian Type; LSFC OMIM:256000 Leigh Syndrome; LS OMIM:150700 Leiomyoma of Vulva and Esophagus OMIM[informatics.jax.org] midface hypoplasia Head And Neck Nose: anteverted nares low nasal bridge Head And Neck Eyes: horizontal nystagmus loss of vision Skeletal: decreased bone mineralization Clinical[malacards.org] […] of, with Congenital Cataract OMIM:150600 Legg-Calve-Perthes Disease; LCPD OMIM:608556 Legionnaire Disease, Susceptibility to OMIM:611431 Legius Syndrome; LGSS OMIM:150590 Leg[informatics.jax.org]

  • Dehydration

    […] ptosis, flat midface, flat nasal bridge and upturned nasal tip, short philtrum with a triangular mouth, and thickened, everted lips) and hand anomalies (aplasia or hypoplasia[orpha.net] Clinical description Typical facial features include wide-set eyes, downslanting palpebral fissures, mild ptosis, flat midface, flat nasal bridge, upturned nasal tip, a short[orpha.net] […] congenital anomalies/dysmorphic syndrome characterized by the triad of patent ductus arteriosus (PDA), facial dysmorphism (wide-set eyes, downslanting palpebral fissures, mild[orpha.net]

    Missing: Juvenile Familial Leg Ulcers
  • Crouzon Syndrome

    For the patient with mild midface hypoplasia, good nasal profile, and malocclusion, rib bone graft along with Le Fort I and bilateral sagittal ramus osteotomy can be a good[ncbi.nlm.nih.gov] The appearance of an infant with Crouzon's syndrome can vary in severity from a mild presentation with subtle midface characteristics to a severe form with multiple cranial[skullbaseinstitute.com] The characteristic features of Crouzon's syndrome are ocular proptosis (exophthalmos), maxillary hypoplasia, excessive distance between both eyes (orbital hypertelorism) and[skullbaseinstitute.com]

    Missing: Juvenile Familial Leg Ulcers
  • Coxa Valga

    hypoplasia, and mild intellectual disability.[ncbi.nlm.nih.gov] Anauxetic dysplasia is a spondyloepimetaphyseal dysplasia characterized by severe short stature of prenatal onset, very short adult height (less than 1 meter), hypodontia, midface[ncbi.nlm.nih.gov]

    Missing: Juvenile Familial Leg Ulcers
  • Congenital Mandibular Hypoplasia

    hypoplasia, mild microcephaly, short hard palate, small nose with flat nasal bridge, protruding tongue MSK - short metacarpals/phalanges, wide-spaced 1st/2nd toes, short[quizlet.com] Pelvic dysplasia Other feats: Craniofacial - brachycephaly, flat occiput, prominent epicanthal folds, speckled irises (Brushfield spots), 3 fontanelles with delayed closure, midface[quizlet.com]

    Missing: Juvenile Familial Leg Ulcers
  • X-linked Distal Spinal Muscular Atrophy Type 3

    hypoplasia), audiologic (hearing loss), and joint abnormalities (early arthritis, mild spondlyepiphyseal dysplasia).[chginc.org] […] connective tissue disorder that includes ophthalmologic (myopia, cataract, and retinal detachment), craniofacial (Pierre Robin sequence: micrognathia, glossoptosis, cleft palate, midface[chginc.org]

    Missing: Juvenile Familial Leg Ulcers
  • Craniosynostosis

    […] year-old female patient with Antely-Bixler syndrome) with mild midface hypoplasia without malocclusion.[ncbi.nlm.nih.gov] hypoplasia—usually mild Wide set eyes Low set ears Broad toes, brachydactyly Potential developmental delay Usually mild compared with other syndromic forms but higher risk[academic.oup.com] Perinasal osteotomy was performed with distraction osteogenesis to move the midface forward in 2 patients (a 17-year old female patient with Crouzon-like disease and a 15-[ncbi.nlm.nih.gov]

    Missing: Juvenile Familial Leg Ulcers
  • Subcortical Band Heterotopia

    hypoplasia, bilateral punctate cataract, microretrognathia, short neck, pectus excavatum, joint hypermobility, mild muscular hypotonia, generalized seizures, and mild mental[ncbi.nlm.nih.gov] […] a severe and diffuse mosaic skin hypopigmentation running (in narrow bands) along the lines of Blaschko associated with mosaic areas of alopecia, facial dysmorphism with midface[ncbi.nlm.nih.gov]

    Missing: Juvenile Familial Leg Ulcers
  • Cloverleaf Skull

    Type 1 involves individuals with mild manifestations including brachycephaly, midface hypoplasia and finger and toe abnormalities.[genome.jp] Type 1 "classic" Pfeiffer syndrome involves individuals with mild manifestations including brachycephaly, midface hypoplasia and finger and toe abnormalities; it is associated[ojrd.biomedcentral.com] Figure 30-10 A 15-year-old girl with Crouzon syndrome that is characterized by mild to moderate midface deficiency with retrusion of the infraorbital rims, the zygomatic buttresses[pocketdentistry.com]

    Missing: Juvenile Familial Leg Ulcers
  • Craniofacial Dyssynostosis
    Missing: Juvenile Familial Leg Ulcers

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