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141 Possible Causes for Delayed Speech and Language Development, Poor Feeding, Round Face

  • Prader-Willi Syndrome

    Speech and language therapy during childhood will help with impaired speech and delay in developing language.[yourhormones.info] (menkes, textbook of child neurology, 5th ed, p229) Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism[icd9data.com] Prader-Willi syndrome (PWS) is characterized by infantile lethargy and hypotonia causing poor feeding and failure to thrive, childhood obesity, short stature, and hypogonadism[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis

    OBJECTIVE: To evaluate the efficacy and safety of IV laronidase for MPS I. METHODS: A systematic literature review was performed by searching the ClinicalTrials.gov, MEDLINE/PubMed, EMBASE, LILACS, and Cochrane Library databases, limited to clinical trials published until December 31, 2016. The first inclusion criterion[…][ncbi.nlm.nih.gov]

  • Dubowitz Syndrome

    speech and language development Deficiency of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired[rarediseases.info.nih.gov] Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism, hypotonia, insatiable appetite leading to obesity[icd10data.com] feeding.[ncbi.nlm.nih.gov]

  • Mandibulofacial Dysostosis

    speech and language development Deficiency of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired[rarediseases.info.nih.gov] The hallmarks of the syndrome are a round, flat face, severe hypertelorism, downslanting palpebral fissures extending to the temples, a broad nasal base, anteverted nares,[ncbi.nlm.nih.gov] MFDM is caused by mutations in the EFTUD2 gene and is inherited in an autosomal dominant manner. 0000750 Feeding difficulties Feeding problems Poor feeding Last updated: 7[rarediseases.info.nih.gov]

  • Multicore Myopathy

    speech and language development Cryptorchidism Strabismus Hypokinesia Type 1 muscle fiber predominance Abnormality of the thorax Dysphagia Milia Increased connective tissue[mendelian.co] […] with external ophthalmoplegia * Neonatal hypotonia * Delayed motor development * Muscle weakness * Amyotrophy * Paralysis of external eye muscles * High arched palate * Poor[checkorphan.org] .  Facial dysmorphism is common and includes micrognathia, a round face with drooping of the lower lids, and prominent ears.  Skin changes can include follicular hyperkeratosis[slideshare.net]

  • Pallister W Syndrome

    Children have a round face, with wide eyebrows and mild synophrys, hypertelorism, a prominent and high nasal bridge with anteverted nostrils, a long philtrum and a thin upper[ojrd.biomedcentral.com] Clinical diagnosis is based on a variety of characteristics common to Williams syndrome, including the typical facial features, heart problems, poor feeding and developmental[contact.org.uk] face and developmental delay syndrome (disorder) {715987000, SNOMED-CT } Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder) {722389002,[phinvads.cdc.gov]

  • Autosomal Dominant Mental Retardation 21

    speech and language development, Infantile muscular hypotonia, Malar flattening, Mandibular prognathia, Misalignment of teeth, Obesity, Poor fine motor coordination, Thin[genecards.org] Affected individuals also have distinctive facial features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face.[tsbvi.edu] Feeding difficulties have been reported while anal atresia is present in about half of patients.[disorders.eyes.arizona.edu]

  • Chromosome 18p Deletion Syndrome

    Speech/Language delay Mostly all individuals with 9p deletions have a significant speech and language delay.[9pminus.org] […] symptoms listed below: * Growth retardation * Mental retardation * Reduced muscle tone * Small head * Drooping eyelids * Epicanthal folds * Low nasal bridge * Wide-set eyes * Round[checkorphan.org] Children with 22q11.2 deletion and duplication syndromes often have other health problems, including: Heart defects Feeding difficulties Gastrointestinal problems Immune system[chop.edu]

  • Neuhauser Syndrome

    BRAIN MYELINATION NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia,[rgd.mcw.edu] The patients have a peculiar face by specific craniofacial anomalies: round face, wide prominent forehead, hypertelorism, broad nasal bridge, bulbous nose, wide philtrum nasolabial[ncbi.nlm.nih.gov] Congenital hypothyroidism was diagnosed early; at the first month, the patient was hospitalized for feeding difficulties and severe hypotonia.[azdoc.site]

  • Autosomal Dominant Mental Retardation 28

    […] some of the following symptoms: Uncommon Symptoms - Between 30% and 50% cases Delayed speech and language development Limb ataxia Babinski sign Cognitive impairment Motor[mendelian.co] face, heart anomalies cry like a cat t or f: sex chromosome disorders are much more drastic and less common false; less drastic, but more common sex chromosome extra x in[studyblue.com] Orofacial clefting, heart defects, short stature, feeding difficulties and hypotonia can be observed.[findzebra.com]

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