Other Growth Disorders

There are hundreds of known medical issues which can impact a child's growth. We have compiled a list of some disorders and included links to other support organizations, if available.  If you need more information pertaining to the conditions on this page, or have a link to another resource for one of the disorders below, feel free to contact us.


Partial List of Disorders Affecting Growth


3M Syndrome
6p25 Chromosome Deletion/ Riegers Anomly (Syndrome)
Aarskog Syndrome
Addisons Disease
Adrenal Disorder
Alagille Syndrome 
Albright Hereditary Osteodystrophy
Angelman Syndrome
Androgen Insensitivity syndrome
Arnold-Chiari Malformation
Asperger Syndrome


Batten Disease Support and Research Association
Behcet's Disease 
Bloom Syndrome 
Bone Dysplasia (resembles Spondyloepiphyseal Dyspl)
Brachytelephalangic Chondrodysplasia Punctata (BCDP)

Campomelic Dysplasia or Syndrome
Cardiofaciocutaneous Syndrome
Cartilage-hair Hypoplasia
Cat Eye Syndrome
Caudal Regression Syndrome
Celiac Disease
Cerebral Palsy
          Cerebral Palsy Group
          Cerebral Palsy Guidance
Charcot-Marie-Tooth Association
Charge Syndrome
Chromosomal disorder 18p-
Chromosome deletion 10 of 26 
Chromosome 22 q 11.2 Deletion  (also called Velo-Cardio-Facial syndrome, Shprintzen Syn, & DiGeorge Sequence)
Cleidocranial Dysostosis
Cockayne Syndrome possible
Conradi Hunermann
Cornelia deLange Syndrome 

  1. http://www.cdlsusa.org/   is the link for the home page of the CdLS Foundation (USA).

  2. http://groups.yahoo.com/group/cdls-kids/   is the link for the home page of the CdLS online support group.

  3. http://www.cdlsworld.org   is the link for the CdLS World Organization 

Costello Syndrome
Crohn's Disease 


DeBarsy Syndrome
Delayed Puberty
Deletion Chromosome 2, possible GHD
Diastrophic Dysplasia
DiGeorge Syndrome
Down Syndrome
Dubowitz Syndrome & CPP
Dyggve Melchior Clausen
Dyslexia Research Society
International Dyslexia Association


Edwards Syndrome
Ehlers-Danlos Syndrome
Empty Sella
Epilepsy Foundation
Epstein-Barr Syndrome 


Failure to Thrive
Fairbank Disease -  Multiple Epiphyseal Dysplasia
Familial Dysautonomia
Fanconi Anemia
Fetal Alcohol Syndrome and Support
Fetal Anti-Convulsant Syndrome
Fetal Veapkote Syndrome / Fetal Balproate Acid Syndrome
Froelich's Syndrome


Gerneralized Resistance to Thyroid Hormone
Geroderma Osteocystlastica
Glycogen Storage Disease
Graves Disease
Guillan Barre Syndrome Foundation


Hallerman-Streif Syndrome
Hashimoto Thyroiditis
Huntington's Disease Society of America
Hydrocephlus - IUGR
Hypocalcemia/Calcium Sensing Receptor Gene Mutation
Hypophospatemic Rickets/AGHD


Idiopathic Short Stature
Inflamatory bowel disease/excessive production of GH
Intrauterine Growth Restriction


Jarcho-Levine Syndrome
Jeune Syndrome
Johanson Blizzard Syndrome
Juenes/Barnes Syndrome possible


Kallmann Syndrome 
Kabuki Syndrome
Kenny Caffey Syndrome
Ketotic Hypoglycemia
Kleinfelters Syndrome
Kniest Syndrome (blog by mom)


Laron Syndrome
Langer Giedion Syndrome Possible
Langerhans cell Histiocytosis
Larsen's Syndrome
Leopard Syndrome
Leri Weill possible
Leukemia/Bone Marrow Transplant/
LGH/Skeletal Dysplasia
Lupus Foundation of America


Mayer Rokinstanski Syndrome
Marshall Smith Syndrome
Meier-Gorlin Syndrome - Ear, Patella, Short Stature-RSS possible
Metaphyseal Chondrodysplasia,type McKusick
Metaphyseal Dysplasia
Mixed Gonadal Dysgenesis
Moebius Syndrome
Morquio Syndrome A
Mulibrey Nanism
Multiple Epiphyseal Dysplasia 


Niemann Pick Disease
Noonan Syndrome


Osteogenesis Imperfecta 


PAIS-Androgen Insensitivity 46xy
Partial Trisomy 10Q
Partial Trisomy 9P
Pierre Robin Syndrome/RSS
Pituitary Tumors
Pituitary Stalk Interruption Syndrome-PAN
Prader Willi    USA   or   NY Chapter

Premature Adrenarche (see Precocious Puberty)
Pseudohypoaldosteronism (PHA) 



Reciprocol Translocation of Chromosomes 7 and 9, possible GHD
Rett Syndrome
Rhizomelic Chondrodysplasia Punctata (RCDP)
Robinow Syndrome


Shwachman Diamond Syndrome
Seckel Syndrome
Short Stature
Short Syndrome
Skeletal Dysplasia
Sotos Syndrome
Spina Bifida
Spondyloepiphyseal Dysplasia


Tangiers Syndrome
Trichorhinophalangeal Syndrome
Trisomy 14, Mosaic Pattern
Trisomy 18
Trisomy 21
trisomy 4 P +, GHD, genisis of the corpus colosom, ONH


Weaver Syndrome
Weill Marchesani Syndrome
Williams Syndrome
Wolf-Hirshhorn Syndrome also called 4P Minus 


XQ 2628 Duplication
XXX Syndrome, Triple X Syndrome


Zellweger Syndrome

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