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Beckwith Wiedemann Syndrome
Beckwith wiedemann syndrome
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Genetic disorders
(36)
Apert syndrome
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Benign paroxysmal peritonitis
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
Bardet Biedl Syndrome
WAGR complex
Angelman syndrome
Timothy syndrome
Batten disease
Simpson-Go- labi-Behmel syndrome
Hyperostosis, cortical, congenital
Gastroschisis
Adrenoleuk- odystrophy
Denys-Drash
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Prader Willi syndrome
Vacterl association
Carpenter syndrome
Treacher Collins syndrome
Birt-Hogg-Dube syndrome
Bannayan-R- iley-Ruvalcaba syndrome
Bassen-Kornzweig syndrome
Trisomy 18
Glutaricaciduria
more...
Medical condition
(65)
Omphalocele
Exomphalos- -macroglossia-gigantism syndrome
Blount disease
Wilms tumor
Macroglossia
Macroglossia
Umbilical hernia
Blepharophimosis ptosis epicanthus inversus
Fetofetal transfusion
Glossopharyngeal nerve diseases
Bowen syndrome
Gigantism
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Wildervanck syndrome
Weil syndrome
Wilms tumor and pseudoherm- aphroditism
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Rosenthal syndrome
Windmill-Vane-Hand syndrome
Weismann netter stuhl syndrome
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Floating harbor syndrome
Encephalitis, arbovirus
Olfaction disorders
Brueghel syndrome
Diaphragmatic hernia
Brachial plexus neuropathies
Craniofrontonasal dysplasia
Wiedemann rautenstrauch syndrome
Intervertebral disk displacement
Adrenal carcinoma
Uniparental disomy
Wieacker syndrome
Sotos syndrome
Apert syndrome
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Benign paroxysmal peritonitis
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Donohue syndrome
Branchio-Oto-Renal Syndrome
Bardet Biedl Syndrome
WAGR complex
Angelman syndrome
Timothy syndrome
Batten disease
Hyperostosis, cortical, congenital
Gastroschisis
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Prader Willi syndrome
Vacterl association
Carpenter syndrome
Bassen-Kornzweig syndrome
Trisomy 18
Glutaricaciduria
more...
Genodermatoses
Apert syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Windmill-Vane-Hand syndrome
Treacher Collins syndrome
Genetic disorder
(11)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
Simpson-Go- labi-Behmel syndrome
more...
Autosomal recessive disorders
(12)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Benign paroxysmal peritonitis
Fountain syndrome
Keutel syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Batten disease
Gastroschisis
Leukodystrophy, globoid cell
Carpenter syndrome
Bassen-Kornzweig syndrome
more...
Rare diseases
(15)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Zimmerman Laband syndrome
Aarskog-Scott syndrome
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Angelman syndrome
Denys-Drash
Leukodystrophy, globoid cell
Carpenter syndrome
Treacher Collins syndrome
Birt-Hogg-Dube syndrome
more...
Growth disorders
Silver-Russell dwarfism
Hemihypertrophy
Gigantism
Symptoms
(11)
Creases in ear lobes
Large tongue sometimes protruding
Large newborn
Cryptorchidism
Diastasis recti
Diastasis recti
Dysphagia
External ear (pinna) abnormalities and low-set ears
Fatigue (medical)
Gestational age
Seizure
Separated abdominal muscles
more...
Causes, incidence, and risk factors
Chromosome
Hypoglycemia
Tumor
Wilms' tumor
Signs and tests
A ridge in the forehead caused by premature closure of the bones (metopic ridge)
CT scan of the abdomen
Long bone
Magnetic resonance imaging
X-ray
X-ray of the abdomen
See also
(20)
Diseases and disorders
Beta HCG
Bioaccumulants
Genomic imprinting
Biological magnification
Biological magnification
Weaver syndrome
Macrosomia
Overgrowth syndrome
Chromosome 11
Brainwave entrainment
Christian Rudolph Wilhelm Wiedemann
Polyhydramnios
CDKN1C
KCNQ1OT1
IGF2
Epigenetic
Mucopolysaccharide
Persistent thyroglossal duct
H19 (gene)
Intravenous therapy
more...
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