Syndactyly
Disease Information
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Poland syndactyly: A unique pattern of one-sided malformations characterized by a defect of the chest (pectoralis) muscle on one side of the body and webbing of the fingers (cutaneous syndactyly) of the ipsilateral hand ...
Syndactyly
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Symptoms, Diagnosis & Tests ...
GCPS
Polysyndactyly with Peculiar Skull Shape
Polysyndactyly-Dysmorphic Craniofacies, Greig Type
Frontodigital Syndrome (obsolete)
Hootnick-Holmes Syndrome (obsolete) ...
cephalopolysyndactyly syndrome
Greig cephalopolysyndactyly (GCPS) syndrome
Greig syndrome
See How are genetic conditions and genes named? in the Handbook.
Aphalangia syndactyly microcephaly
Overview
Aphalangia - syndactyly - microcephaly: A very rare syndrome characterized by the absence of one or more bones of the fingers and toes, a small head and fusion of fingers.
Acrocephalosyndactyly
condition in which primary craniosynostoses of the Coronal: \r\n An orthogonal plane of the body that passes vertically through the body from left to right.
syndactyly - a congenital problem characterized by a union of fingers or toes.
syndromic hearing impairment - hearing loss or deafness that is inherited or passed through generations of a family.
Polysyndactyly: a rare development disorder. Patients have additional and webbed toes, and heart defects.
Syndactyly may be discovered during an examination of an infant or child. In its most common form, it is seen as webbing between the second and third toes. This form is often inherited and is not unusual.
Syndactyly
Reviewed last on: 7/1/2007
Brian Kirmse, MD, Mount Sinai School of Medicine, Department of HumanGenetics, New York, NY. Review provided by VeriMed Healthcare Network.
Acrocephalosyndactyly type I
Signs and Symptoms
The spectrum of abnormalities in Apert syndrome has recently been described along with current recommendations for orthodontic treatment.
Acrocephalosyndactyly, Acrocephalosyndactyly type 1, acrocephaly, ASC 1, autosomal dominant trait, craniosurgery, craniosynostosis, FGFR2 gene, fibroblast growth factor receptor 2, fibroblast growth factor receptor 2 gene, intellectual disabilities, ...
Acrocephalosyndactyly
Causes
Apert syndrome can be passed down through families (inherited).
ACROCEPHALOSYNDACTYLY TYPE 1
2:
Discovery Health "Apert Syndrome - Medical Dictionary" ...
acrocephalosyndactyly, type V
ACSV
Noack syndrome
craniofacial-skeletal-dermatologic syndrome ...
Polydactyly/Syndactyly (Webbed toes)
reduction deficits (Ectrodactyly, Amelia, Phocomelia)
upper limb (Cleidocranial dysostosis, Madelung's deformity, Sprengel's deformity) ...
AcrocephalosyndactylyAn inherited disorder causing abnormalities of the skull and face and the hands and feet. In acrocephalosyndactyly there is closure too-early of some of the sutures of the skull (craniosynostosis).
Acrocephalopolysyndactyly, type 2 (ACPS 2) ... speech problems
Acrofacial dysostosis, Nager type ... delayed speech development
B ...
Aux-, Acrocephalosyndactyly, ACL, Dequalinium Diundecenoate, Economics, Economics, Medical, Gene, Plant, Health Services, National, Hemihydrate, Thioguanine, Hereditary Sensory Neuropathy, Dominant, Type III, Hispanic American, Isometric Contractions, ...
Greig Cephalopolysyndactyly Syndrome
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Grief and PTSD
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Grief, Bereavement, and Coping With Loss (PDQ®): Supportive care - Health Professional Information [NCI] ...
Goodman syndrome: A genetic syndrome characterized by acrocephalosyndactyly - birth defects involving the head and face and the fingers.
Other more moderate limb defects that have been reported include webbing (syndactyly) of the skin (cutaneous syndactyly) or bones (bony syndactyly) of the fingers or toes, claw-hand malformation (ectrodactly), ...
Definition Polydactyly and syndactyly are congenital malformations of the fingers and/or toes. Polydactylyis the presence of extra fingers or toes, and syndactyly is the fusing together or webbing of two or more fingers or toes.
Malformations of the hands and feet - including missing thumbs, club feet and webbing between the fingers and toes (syndactyly).
Congenital malformation in which oxycephaly, brachysyndactyly of hand, and preaxial polydactyly of feet are associated with mental retardation; it is usually inherited as an autosomal recessive trait but there is also a dominant form.
Microcephalus-imperforate Anus-syndactyly-hamartoblastoma-abnormal Lung Lobulation-polydactyly [syndrome]
IBAT
Intravascular Bronchoalveolar Tumor ...
The severe generalized subtype, associated with formation of pseudosyndactyly (a mitten-like deformity secondary to fusion of interdigital webbing) in early childhood, carries a SCC risk of up to 85% by the age of 45.
Cutaneous or bony syndactyly of the 2nd and 3rd fingers distinguishes sclerosteosis from other forms of craniotubular hyperostoses. Predominant x-ray study features are gross widening and sclerosis of the calvaria and mandible.
Syndactyly without fusion of bone
Dermatoglyphic anomalies
Vascular hamartomas
Congenital pigmentation anomalies of skin
Other anomalies of skin
Specified anomalies of hair
Specified anomalies of nails
Specified anomalies of breast ...
Poland syndrome is noted for the underdevelopment or absence of the chest (pectoralis) muscles on one side of the body as well as webbing of the fingers (cutaneous syndactyly) on the hand of the same side (ipsilateral side) of the body.
Scaphoid Fractures
Swan Neck Deformity
Syndactyly of the Hand
Thumb Ulnar Collateral Ligament (UCL) Injury
Triangular Fibrocartilage Complex (TFCC) Tears
Trigger Digit
Volar Plate Injuries
Wrist Sprain ...
 See also: Symptom, Fusion, Autosomal dominant, Cancer, Autosomal recessive
  
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