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14 Possible Causes for Failure to Thrive, Overfolded Superior Helix

  • Propionic Acidemia

    There was mild plagiocephaly and overfolding of the superior helix of each ear. The lower lip had loss of tissue in 2 lateral clefts with bulbous tissue in the center.[] A 15-month-old girl with propionic acidemia presented a failure to thrive and muscular hypotonia, who had been treated with diets low in leucine, valine, isoleucine, threonine[] In the chronic progressive form, the disease presents as failure to thrive, chronic vomiting, psychomotor delay, hypotonia, seizures and movement disorders.[]

  • Kaufman Oculocerebrofacial Syndrome

    Symptoms INHERITANCE: Autosomal dominant HEAD AND NECK: [Head]; Open metopic suture; [Face]; Midface hypoplasia; Micrognathia; [Ears]; Low-set ears; Overfolded superior helix[] thrive, eye abnormalities, other congenital malformations, low cholesterol levels, and severe intellectual disability.[] […] to thrive / difficulties for feeding in infancy / growth delay - High vaulted / narrow palate - Long face - Macrostomia / big mouth - Microcornea - Muscle weakness / flaccidity[]

  • Baller-Gerold Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] […] of the radius 0006501 Aplasia/Hypoplasia of the thumb Absent/small thumb Absent/underdeveloped thumb [ more ] 0009601 Brachyturricephaly High, prominent forehead 0000244 Failure[] At an older age (patient 4 at 3 and 6 years), dysmorphia is less pronounced but failure to thrive is obvious.[]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[] Other findings can include failure to thrive, feeding difficulties, short stature, ophthalmologic abnormalities, microcephaly and hearing loss.[] […] macrocephaly; constipation that may be associated with anal anomalies; broad thumbs and halluces; prominent fingertip pads; and small, rounded, cupped ears that often have an overfolded[]

  • Camptodactyly Syndrome Guadalajara Type 1

    The complications of Camptodactyly Syndrome, Guadalajara Type 1 may include: Failure to thrive after birth Delay in achieving developmental milestones Trauma/injury: Seizures[] […] to thrive Flexion contracture SOURCES: ORPHANET UMLS MONDO OMIM MESH More info about SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE Low match GERODERMA OSTEODYSPLASTICUM[] […] to thrive Postnatal growth retardation Absent palmar crease Short femoral neck Moderately short stature Cigarette-paper scars Thenar muscle atrophy Flattened epiphysis Flat[]

  • Pallister W Syndrome

    […] main genetic causes and other rarer cause of PWS all involving chromosome 15 give rise to a pattern of atypical early development characterised by extreme floppiness and failure[] superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] Hypercalcaemia may cause failure to thrive, feeding problems, irritability, vomiting, constipation and kidney problems.[]

  • Auriculocondylar Syndrome

    Narrow mouth Overfolding of the superior helices Postauricular skin tag Posteriorly rotated ears Preauricular skin tag Round face Stenosis of the external auditory canal[] […] to thrive.[] […] to thrive. 37, 38 General anesthesia can be problematic due to problems with intubation.[]

  • Uncombable Hair Syndrome

    helix Short chin Myopathic facies Inverted nipples Pain insensitivity Horizontal eyebrow Oval face Overfolding of the superior helices Broad chin Micrognathia Neurological[] […] to thrive, slightly prolonged neonatal jaundice, equivocal or mild hepatomegaly, microcytic anemia, frequent upper respiratory infections, gastroenteritis, dehydration and[] Broad nasal tip Long face Deeply set eye Delayed myelination Decreased fetal movement Apraxia Muscular hypotonia of the trunk Stereotypy Deep philtrum Poor head control Overfolded[]

  • Chudley-McCullough Syndrome

    helix Narrow palpebral fissure Aortic aneurysm Aortic regurgitation Interrupted aortic arch Abnormality of earlobe Sandal gap Cardiomyopathy Coarse facial features Congenital[] […] pigmented nevus; gmn; giant congenital melanocytic nevus; giant pigmented hairy nevus; lcmn Related symptoms: Autosomal dominant inheritance Seizures Pica Hypertelorism Failure[] […] to thrive, developmental delay, liver dysfunction, and abnormal subcortical white matter A #175100 Familial adenomatous polyposis 1 (FAP1) M #614937 Familial Cortical Myoclonus[]

  • Homozygous 11p15-p14 Deletion Syndrome

    helix Central apnea Ankylosis Upper airway obstruction Long penis Neurodevelopmental delay Poroma Snoring Overfolding of the superior helices Speech articulation difficulties[] • Concept ID: C0231246 • Finding Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm.[] […] dysplasia Abnormality of vision Abnormal palate morphology 2-3 toe syndactyly Facial cleft External ear malformation Short philtrum Protruding ear Hydrocele testis Hypoplastic superior[]

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